nsv4374272

Organism: Homo sapiens

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

Variant Calls:58
Validation:Not tested
Clinical Assertions: No
Region Size:93,096

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: 553 SVs from 55 studies. See in: genome view

Remapped(Score: Perfect):54,934,156-55,027,251

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4374272	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nsv4374272	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000011.9	Chr11	54,701,632	54,794,727

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv15613129	copy number gain	1-0677-001	SNP array	Genotyping	26
nssv15618804	copy number gain	1-0171-004	SNP array	Genotyping	30
nssv15626593	copy number gain	1-0447-001	SNP array	Genotyping	23
nssv15626971	copy number gain	1-0458-003	SNP array	Genotyping	25
nssv15628586	copy number gain	1-0538-001	SNP array	Genotyping	18
nssv15631661	copy number gain	10-0013-001	SNP array	Genotyping	25
nssv15637425	copy number gain	13-0095-002	SNP array	Genotyping	22
nssv15637461	copy number gain	13-0095-004	SNP array	Genotyping	24
nssv15640617	copy number gain	14-0344-003	SNP array	Genotyping	33
nssv15642762	copy number gain	14-0361-001	SNP array	Genotyping	15
nssv15643194	copy number gain	14-0361-003	SNP array	Genotyping	21
nssv15657149	copy number gain	3-0021-000	SNP array	Genotyping	26
nssv15664306	copy number gain	7-0054-003	SNP array	Genotyping	38
nssv15666104	copy number gain	5-0084-002	SNP array	Genotyping	18
nssv15666251	copy number gain	5-0106-001	SNP array	Genotyping	20
nssv15673101	copy number gain	9-0027-002	SNP array	Genotyping	22
nssv15673146	copy number gain	9-0028-003	SNP array	Genotyping	16
nssv15674012	copy number gain	9-0030-003	SNP array	Genotyping	20
nssv15682648	copy number gain	OCD1126-B_1628	SNP array	Genotyping	13
nssv15682662	copy number gain	OCD1127-715	SNP array	Genotyping	18
nssv15682936	copy number gain	OCD120-B_1732	SNP array	Genotyping	28
nssv15682965	copy number gain	OCD120-S_1733	SNP array	Genotyping	23
nssv15683208	copy number gain	OCD1002-S_896873	SNP array	Genotyping	20
nssv15683234	copy number gain	OCD1007-S_0625-5706-3	SNP array	Genotyping	19
nssv15683440	copy number gain	OCD124-B_188563	SNP array	Genotyping	28
nssv15683488	copy number gain	OCD124-S_OC-4121	SNP array	Genotyping	24
nssv15684004	copy number gain	OCD146-JS-1254(188613)	SNP array	Genotyping	20
nssv15684517	copy number gain	OCD14-S_896271	SNP array	Genotyping	22
nssv15685339	copy number gain	OCD118-B_1711	SNP array	Genotyping	16
nssv15685378	copy number gain	OCD118-S_1713	SNP array	Genotyping	18
nssv15685395	copy number gain	OCD119-B_1726	SNP array	Genotyping	23
nssv15685417	copy number gain	OCD119-B_1727	SNP array	Genotyping	18
nssv15686155	copy number gain	OCD2-B_MA-1288	SNP array	Genotyping	21
nssv15686270	copy number gain	OCD3-S_896083	SNP array	Genotyping	27
nssv15687044	copy number gain	OCD39-S_0625-1152-2	SNP array	Genotyping	27
nssv15687241	copy number gain	OCD4-S_896091	SNP array	Genotyping	23
nssv15687404	copy number gain	OCD48-0625-6045-2	SNP array	Genotyping	22
nssv15687414	copy number gain	OCD49-0625-7114-2	SNP array	Genotyping	24
nssv15688729	copy number gain	OCD46-0625-5375-1	SNP array	Genotyping	21
nssv15688764	copy number gain	OCD46-S_0625-5375-3	SNP array	Genotyping	16
nssv15688829	copy number gain	OCD48-0625-6045-3	SNP array	Genotyping	20
nssv15689555	copy number gain	OCD111-S_1657	SNP array	Genotyping	25
nssv15690018	copy number gain	OCD1163-0625-7948-2	SNP array	Genotyping	22
nssv15690427	copy number gain	OCD143-DH-1299(189273)	SNP array	Genotyping	21
nssv15691492	copy number gain	OCD44-B_KH-1375	SNP array	Genotyping	19
nssv15693016	copy number gain	OCD8-S_896143	SNP array	Genotyping	27
nssv15693640	copy number gain	OCD98-1526	SNP array	Genotyping	26
nssv15693808	copy number gain	OCD70-896291	SNP array	Genotyping	24
nssv15697743	copy number gain	176440	SNP array	Genotyping	17
nssv15698308	copy number gain	139979	SNP array	Genotyping	26
nssv15698363	copy number gain	165194	SNP array	Genotyping	29
nssv15698415	copy number gain	177296	SNP array	Genotyping	18
nssv15699620	copy number gain	168766	SNP array	Genotyping	24
nssv15700040	copy number gain	178856	SNP array	Genotyping	14
nssv15700945	copy number gain	228960	SNP array	Genotyping	28
nssv15701162	copy number gain	178898	SNP array	Genotyping	13
nssv15701775	copy number gain	170722	SNP array	Genotyping	24
nssv15702654	copy number gain	195910	SNP array	Genotyping	19

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv15613129	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15618804	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15626593	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15626971	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15628586	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15631661	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15637425	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15637461	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15640617	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15642762	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15643194	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15657149	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15664306	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15666104	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15666251	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15673101	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15673146	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15674012	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15682648	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15682662	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15682936	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15682965	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15683208	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15683234	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15683440	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15683488	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15684004	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15684517	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15685339	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15685378	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15685395	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15685417	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15686155	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15686270	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15687044	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15687241	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15687404	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15687414	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15688729	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15688764	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15688829	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15689555	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15690018	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15690427	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15691492	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15693016	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15693640	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15693808	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15697743	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15698308	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15698363	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15698415	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15699620	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15700040	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15700945	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15701162	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15701775	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15702654	Remapped	Perfect	NC_000011.10:g.(?_ 54934156)_(5502725 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	54,934,156	55,027,251
nssv15613129	Submitted genomic		NC_000011.9:g.(?_5 4701632)_(54794727 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	54,701,632	54,794,727
nssv15618804	Submitted genomic		NC_000011.9:g.(?_5 4701632)_(54794727 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	54,701,632	54,794,727
nssv15626593	Submitted genomic		NC_000011.9:g.(?_5 4701632)_(54794727 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	54,701,632	54,794,727
nssv15626971	Submitted genomic		NC_000011.9:g.(?_5 4701632)_(54794727 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	54,701,632	54,794,727
nssv15628586	Submitted genomic		NC_000011.9:g.(?_5 4701632)_(54794727 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	54,701,632	54,794,727
nssv15631661	Submitted genomic		NC_000011.9:g.(?_5 4701632)_(54794727 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	54,701,632	54,794,727
nssv15637425	Submitted genomic		NC_000011.9:g.(?_5 4701632)_(54794727 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	54,701,632	54,794,727
nssv15637461	Submitted genomic		NC_000011.9:g.(?_5 4701632)_(54794727 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	54,701,632	54,794,727
nssv15640617	Submitted genomic		NC_000011.9:g.(?_5 4701632)_(54794727 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	54,701,632	54,794,727
nssv15642762	Submitted genomic		NC_000011.9:g.(?_5 4701632)_(54794727 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	54,701,632	54,794,727
nssv15643194	Submitted genomic		NC_000011.9:g.(?_5 4701632)_(54794727 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	54,701,632	54,794,727
nssv15657149	Submitted genomic		NC_000011.9:g.(?_5 4701632)_(54794727 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	54,701,632	54,794,727
nssv15664306	Submitted genomic		NC_000011.9:g.(?_5 4701632)_(54794727 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	54,701,632	54,794,727
nssv15666104	Submitted genomic		NC_000011.9:g.(?_5 4701632)_(54794727 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	54,701,632	54,794,727
nssv15666251	Submitted genomic		NC_000011.9:g.(?_5 4701632)_(54794727 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	54,701,632	54,794,727
nssv15673101	Submitted genomic		NC_000011.9:g.(?_5 4701632)_(54794727 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	54,701,632	54,794,727
nssv15673146	Submitted genomic		NC_000011.9:g.(?_5 4701632)_(54794727 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	54,701,632	54,794,727
nssv15674012	Submitted genomic		NC_000011.9:g.(?_5 4701632)_(54794727 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	54,701,632	54,794,727
nssv15682648	Submitted genomic		NC_000011.9:g.(?_5 4701632)_(54794727 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	54,701,632	54,794,727
nssv15682662	Submitted genomic		NC_000011.9:g.(?_5 4701632)_(54794727 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	54,701,632	54,794,727
nssv15682936	Submitted genomic		NC_000011.9:g.(?_5 4701632)_(54794727 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	54,701,632	54,794,727
nssv15682965	Submitted genomic		NC_000011.9:g.(?_5 4701632)_(54794727 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	54,701,632	54,794,727
nssv15683208	Submitted genomic		NC_000011.9:g.(?_5 4701632)_(54794727 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	54,701,632	54,794,727
nssv15683234	Submitted genomic		NC_000011.9:g.(?_5 4701632)_(54794727 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	54,701,632	54,794,727
nssv15683440	Submitted genomic		NC_000011.9:g.(?_5 4701632)_(54794727 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	54,701,632	54,794,727
nssv15683488	Submitted genomic		NC_000011.9:g.(?_5 4701632)_(54794727 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	54,701,632	54,794,727
nssv15684004	Submitted genomic		NC_000011.9:g.(?_5 4701632)_(54794727 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	54,701,632	54,794,727
nssv15684517	Submitted genomic		NC_000011.9:g.(?_5 4701632)_(54794727 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	54,701,632	54,794,727
nssv15685339	Submitted genomic		NC_000011.9:g.(?_5 4701632)_(54794727 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	54,701,632	54,794,727
nssv15685378	Submitted genomic		NC_000011.9:g.(?_5 4701632)_(54794727 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	54,701,632	54,794,727
nssv15685395	Submitted genomic		NC_000011.9:g.(?_5 4701632)_(54794727 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	54,701,632	54,794,727
nssv15685417	Submitted genomic		NC_000011.9:g.(?_5 4701632)_(54794727 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	54,701,632	54,794,727
nssv15686155	Submitted genomic		NC_000011.9:g.(?_5 4701632)_(54794727 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	54,701,632	54,794,727
nssv15686270	Submitted genomic		NC_000011.9:g.(?_5 4701632)_(54794727 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	54,701,632	54,794,727
nssv15687044	Submitted genomic		NC_000011.9:g.(?_5 4701632)_(54794727 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	54,701,632	54,794,727
nssv15687241	Submitted genomic		NC_000011.9:g.(?_5 4701632)_(54794727 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	54,701,632	54,794,727
nssv15687404	Submitted genomic		NC_000011.9:g.(?_5 4701632)_(54794727 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	54,701,632	54,794,727
nssv15687414	Submitted genomic		NC_000011.9:g.(?_5 4701632)_(54794727 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	54,701,632	54,794,727
nssv15688729	Submitted genomic		NC_000011.9:g.(?_5 4701632)_(54794727 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	54,701,632	54,794,727
nssv15688764	Submitted genomic		NC_000011.9:g.(?_5 4701632)_(54794727 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	54,701,632	54,794,727
nssv15688829	Submitted genomic		NC_000011.9:g.(?_5 4701632)_(54794727 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	54,701,632	54,794,727
nssv15689555	Submitted genomic		NC_000011.9:g.(?_5 4701632)_(54794727 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	54,701,632	54,794,727

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dbVar

Database of genomic structural variation

nsv4374272

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Variant Region Placement Information

Variant Call Information

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