nsv4367151

Organism: Homo sapiens

Study:nstd173 (Zarrei et al. 2019)
Variant Type:copy number variation
Method Type:SNP array
Submitted on:GRCh37 (hg19)

Variant Calls:67
Validation:Not tested
Clinical Assertions: No
Region Size:20,404

Publication(s):Zarrei et al. 2019

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 790 SVs from 91 studies. See in: genome view

Remapped(Score: Perfect):18,919,650-18,940,053

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4367151	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nsv4367151	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000011.9	Chr11	18,941,197	18,961,600

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv15611572	copy number loss	1-0112-001	SNP array	Genotyping	16
nssv15613637	copy number loss	1-0700-006	SNP array	Genotyping	19
nssv15614773	copy number gain	1-0756-002	SNP array	Genotyping	17
nssv15619609	copy number gain	1-0186-001	SNP array	Genotyping	17
nssv15620606	copy number loss	1-0975-003	SNP array	Genotyping	25
nssv15623275	copy number loss	1-0228-005	SNP array	Genotyping	25
nssv15623572	copy number gain	1-0269-003	SNP array	Genotyping	20
nssv15624200	copy number loss	1-0262-002	SNP array	Genotyping	28
nssv15625327	copy number gain	1-0318-004	SNP array	Genotyping	20
nssv15627357	copy number gain	1-0059-002	SNP array	Genotyping	19
nssv15627975	copy number gain	1-0514-005	SNP array	Genotyping	12
nssv15628103	copy number gain	1-0059-003	SNP array	Genotyping	14
nssv15629208	copy number loss	1-0566-001	SNP array	Genotyping	23
nssv15629775	copy number gain	1-0578-003	SNP array	Genotyping	24
nssv15631755	copy number loss	10-0015-001	SNP array	Genotyping	21
nssv15631875	copy number gain	10-1120-002	SNP array	Genotyping	19
nssv15634075	copy number loss	11-0023-003	SNP array	Genotyping	24
nssv15637478	copy number gain	14-0044-002	SNP array	Genotyping	25
nssv15637747	copy number loss	14-0170-001	SNP array	Genotyping	29
nssv15638032	copy number loss	14-0063-002	SNP array	Genotyping	24
nssv15638078	copy number loss	14-0063-004	SNP array	Genotyping	16
nssv15638757	copy number gain	14-0033-001	SNP array	Genotyping	20
nssv15642035	copy number gain	15-1128-001	SNP array	Genotyping	25
nssv15645390	copy number loss	2-0171-003	SNP array	Genotyping	22
nssv15646703	copy number loss	2-0305-003	SNP array	Genotyping	17
nssv15646774	copy number gain	2-0309-005	SNP array	Genotyping	16
nssv15650105	copy number gain	2-1295-001	SNP array	Genotyping	13
nssv15652209	copy number gain	2-1524-003	SNP array	Genotyping	12
nssv15652468	copy number gain	2-1519-006	SNP array	Genotyping	20
nssv15653833	copy number gain	2-1568-001	SNP array	Genotyping	27
nssv15655097	copy number gain	2-1686-003	SNP array	Genotyping	23
nssv15656540	copy number gain	2-1756-003	SNP array	Genotyping	17
nssv15656955	copy number gain	3-0668-000	SNP array	Genotyping	24
nssv15657941	copy number loss	3-0442-000	SNP array	Genotyping	17
nssv15663576	copy number loss	5-1000-001	SNP array	Genotyping	21
nssv15667857	copy number gain	7-0132-003	SNP array	Genotyping	20
nssv15668958	copy number gain	7-0104-002	SNP array	Genotyping	19
nssv15669201	copy number loss	7-0140-003	SNP array	Genotyping	24
nssv15670517	copy number loss	7-0177-003	SNP array	Genotyping	19
nssv15671373	copy number gain	7-0282-003	SNP array	Genotyping	20
nssv15672339	copy number gain	7-0313-003	SNP array	Genotyping	29
nssv15674011	copy number gain	9-0030-003	SNP array	Genotyping	20
nssv15675108	copy number gain	219363	SNP array	Genotyping	20
nssv15675662	copy number gain	9-0045-002	SNP array	Genotyping	22
nssv15675738	copy number gain	172009	SNP array	Genotyping	26
nssv15676423	copy number gain	232816S	SNP array	Genotyping	17
nssv15677574	copy number loss	215804	SNP array	Genotyping	29
nssv15679227	copy number gain	227875	SNP array	Genotyping	22
nssv15679382	copy number loss	219842	SNP array	Genotyping	19
nssv15680708	copy number loss	216162	SNP array	Genotyping	23
nssv15680978	copy number loss	181225	SNP array	Genotyping	16
nssv15681240	copy number gain	214415S	SNP array	Genotyping	18
nssv15681586	copy number loss	240260S	SNP array	Genotyping	30
nssv15682257	copy number loss	235983S	SNP array	Genotyping	43
nssv15682426	copy number loss	OCD1111-896063	SNP array	Genotyping	17
nssv15683569	copy number gain	OCD130-8961052	SNP array	Genotyping	20
nssv15689509	copy number gain	OCD106-1607(313)	SNP array	Genotyping	23
nssv15689605	copy number gain	OCD1115-0625-1325-3	SNP array	Genotyping	14
nssv15689653	copy number loss	OCD1120-896013	SNP array	Genotyping	22
nssv15690119	copy number gain	OCD126-896903	SNP array	Genotyping	19
nssv15692235	copy number gain	OCD67-896283	SNP array	Genotyping	15
nssv15692703	copy number gain	OCD54-0625-8740-1	SNP array	Genotyping	16
nssv15695353	copy number gain	159370	SNP array	Genotyping	26
nssv15695808	copy number gain	207516	SNP array	Genotyping	14
nssv15696607	copy number loss	162332	SNP array	Genotyping	16
nssv15699511	copy number loss	155498	SNP array	Genotyping	20
nssv15700365	copy number gain	205282	SNP array	Genotyping	25

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv15611572	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15613637	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15614773	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15619609	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15620606	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15623275	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15623572	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15624200	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15625327	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15627357	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15627975	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15628103	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15629208	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15629775	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15631755	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15631875	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15634075	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15637478	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15637747	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15638032	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15638078	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15638757	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15642035	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15645390	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15646703	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15646774	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15650105	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15652209	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15652468	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15653833	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15655097	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15656540	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15656955	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15657941	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15663576	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15667857	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15668958	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15669201	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15670517	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15671373	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15672339	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15674011	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15675108	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15675662	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15675738	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15676423	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15677574	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15679227	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15679382	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15680708	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15680978	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15681240	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15681586	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15682257	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15682426	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15683569	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15689509	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15689605	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15689653	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15690119	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15692235	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15692703	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15695353	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15695808	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15696607	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15699511	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15700365	Remapped	Perfect	NC_000011.10:g.(?_ 18919650)_(1894005 3_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	18,919,650	18,940,053
nssv15611572	Submitted genomic		NC_000011.9:g.(?_1 8941197)_(18961600 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	18,941,197	18,961,600
nssv15613637	Submitted genomic		NC_000011.9:g.(?_1 8941197)_(18961600 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	18,941,197	18,961,600
nssv15614773	Submitted genomic		NC_000011.9:g.(?_1 8941197)_(18961600 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	18,941,197	18,961,600
nssv15619609	Submitted genomic		NC_000011.9:g.(?_1 8941197)_(18961600 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	18,941,197	18,961,600
nssv15620606	Submitted genomic		NC_000011.9:g.(?_1 8941197)_(18961600 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	18,941,197	18,961,600
nssv15623275	Submitted genomic		NC_000011.9:g.(?_1 8941197)_(18961600 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	18,941,197	18,961,600
nssv15623572	Submitted genomic		NC_000011.9:g.(?_1 8941197)_(18961600 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	18,941,197	18,961,600
nssv15624200	Submitted genomic		NC_000011.9:g.(?_1 8941197)_(18961600 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	18,941,197	18,961,600
nssv15625327	Submitted genomic		NC_000011.9:g.(?_1 8941197)_(18961600 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	18,941,197	18,961,600
nssv15627357	Submitted genomic		NC_000011.9:g.(?_1 8941197)_(18961600 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	18,941,197	18,961,600
nssv15627975	Submitted genomic		NC_000011.9:g.(?_1 8941197)_(18961600 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	18,941,197	18,961,600
nssv15628103	Submitted genomic		NC_000011.9:g.(?_1 8941197)_(18961600 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	18,941,197	18,961,600
nssv15629208	Submitted genomic		NC_000011.9:g.(?_1 8941197)_(18961600 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	18,941,197	18,961,600
nssv15629775	Submitted genomic		NC_000011.9:g.(?_1 8941197)_(18961600 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	18,941,197	18,961,600
nssv15631755	Submitted genomic		NC_000011.9:g.(?_1 8941197)_(18961600 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	18,941,197	18,961,600
nssv15631875	Submitted genomic		NC_000011.9:g.(?_1 8941197)_(18961600 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	18,941,197	18,961,600
nssv15634075	Submitted genomic		NC_000011.9:g.(?_1 8941197)_(18961600 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	18,941,197	18,961,600
nssv15637478	Submitted genomic		NC_000011.9:g.(?_1 8941197)_(18961600 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	18,941,197	18,961,600
nssv15637747	Submitted genomic		NC_000011.9:g.(?_1 8941197)_(18961600 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	18,941,197	18,961,600
nssv15638032	Submitted genomic		NC_000011.9:g.(?_1 8941197)_(18961600 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	18,941,197	18,961,600
nssv15638078	Submitted genomic		NC_000011.9:g.(?_1 8941197)_(18961600 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	18,941,197	18,961,600
nssv15638757	Submitted genomic		NC_000011.9:g.(?_1 8941197)_(18961600 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	18,941,197	18,961,600
nssv15642035	Submitted genomic		NC_000011.9:g.(?_1 8941197)_(18961600 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	18,941,197	18,961,600
nssv15645390	Submitted genomic		NC_000011.9:g.(?_1 8941197)_(18961600 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	18,941,197	18,961,600
nssv15646703	Submitted genomic		NC_000011.9:g.(?_1 8941197)_(18961600 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	18,941,197	18,961,600
nssv15646774	Submitted genomic		NC_000011.9:g.(?_1 8941197)_(18961600 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	18,941,197	18,961,600
nssv15650105	Submitted genomic		NC_000011.9:g.(?_1 8941197)_(18961600 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	18,941,197	18,961,600
nssv15652209	Submitted genomic		NC_000011.9:g.(?_1 8941197)_(18961600 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	18,941,197	18,961,600
nssv15652468	Submitted genomic		NC_000011.9:g.(?_1 8941197)_(18961600 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	18,941,197	18,961,600
nssv15653833	Submitted genomic		NC_000011.9:g.(?_1 8941197)_(18961600 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	18,941,197	18,961,600
nssv15655097	Submitted genomic		NC_000011.9:g.(?_1 8941197)_(18961600 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	18,941,197	18,961,600
nssv15656540	Submitted genomic		NC_000011.9:g.(?_1 8941197)_(18961600 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	18,941,197	18,961,600
nssv15656955	Submitted genomic		NC_000011.9:g.(?_1 8941197)_(18961600 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	18,941,197	18,961,600

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dbVar

Database of genomic structural variation

nsv4367151

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Variant Region Placement Information

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Variant Call Placement Information

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant