nsv4365131

Organism: Homo sapiens

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

Variant Calls:54
Validation:Not tested
Clinical Assertions: No
Region Size:569,301

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: 2946 SVs from 96 studies. See in: genome view

Remapped(Score: Good):21,935,993-22,505,293

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4365131	Remapped	Good	GRCh38.p12	Primary Assembly	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nsv4365131	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000014.8	Chr14	22,404,167	22,974,280

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv15624454	copy number gain	1-0298-003	SNP array	Genotyping	28
nssv15625137	copy number gain	1-0375-003	SNP array	Genotyping	15
nssv15627234	copy number gain	1-0057-002	SNP array	Genotyping	20
nssv15631715	copy number gain	10-0014-002	SNP array	Genotyping	26
nssv15634728	copy number gain	12-4404-004	SNP array	Genotyping	25
nssv15638444	copy number gain	14-0135-004	SNP array	Genotyping	33
nssv15639490	copy number gain	14-0231-001	SNP array	Genotyping	25
nssv15641336	copy number gain	14-0318-001	SNP array	Genotyping	25
nssv15641785	copy number gain	14-0276-001	SNP array	Genotyping	18
nssv15643047	copy number gain	14-0325-001	SNP array	Genotyping	29
nssv15655706	copy number gain	2-1703-003	SNP array	Genotyping	16
nssv15669513	copy number gain	7-0264-003	SNP array	Genotyping	19
nssv15669536	copy number gain	7-0265-003	SNP array	Genotyping	20
nssv15670440	copy number gain	7-0173-003	SNP array	Genotyping	31
nssv15674030	copy number gain	9-0031-002	SNP array	Genotyping	20
nssv15674333	copy number gain	9-0034-001	SNP array	Genotyping	28
nssv15674359	copy number gain	9-0034-002	SNP array	Genotyping	27
nssv15674379	copy number gain	9-0034-003	SNP array	Genotyping	21
nssv15674803	copy number gain	206771	SNP array	Genotyping	18
nssv15674824	copy number gain	206775	SNP array	Genotyping	21
nssv15674921	copy number gain	206768	SNP array	Genotyping	20
nssv15675470	copy number gain	154609	SNP array	Genotyping	24
nssv15675975	copy number gain	216579	SNP array	Genotyping	25
nssv15676140	copy number gain	206764	SNP array	Genotyping	16
nssv15676427	copy number gain	232816S	SNP array	Genotyping	17
nssv15676500	copy number gain	236818S	SNP array	Genotyping	16
nssv15677321	copy number gain	242264S	SNP array	Genotyping	22
nssv15677381	copy number gain	244358S	SNP array	Genotyping	20
nssv15678088	copy number gain	242811S	SNP array	Genotyping	17
nssv15678107	copy number gain	245252S	SNP array	Genotyping	27
nssv15678474	copy number gain	204956	SNP array	Genotyping	29
nssv15678590	copy number gain	162338	SNP array	Genotyping	14
nssv15678757	copy number gain	242268S	SNP array	Genotyping	22
nssv15679508	copy number gain	234824S	SNP array	Genotyping	21
nssv15679752	copy number gain	207275	SNP array	Genotyping	20
nssv15680083	copy number gain	208030	SNP array	Genotyping	21
nssv15680355	copy number gain	238144S	SNP array	Genotyping	19
nssv15680714	copy number gain	216162	SNP array	Genotyping	23
nssv15681165	copy number gain	239188S	SNP array	Genotyping	27
nssv15682146	copy number gain	219366	SNP array	Genotyping	19
nssv15683067	copy number gain	238146S	SNP array	Genotyping	16
nssv15687576	copy number gain	OCD164-8961142	SNP array	Genotyping	21
nssv15687979	copy number gain	192221	SNP array	Genotyping	18
nssv15688833	copy number gain	OCD48-0625-6045-3	SNP array	Genotyping	20
nssv15688937	copy number gain	225325	SNP array	Genotyping	19
nssv15689136	copy number gain	232818S	SNP array	Genotyping	23
nssv15690077	copy number gain	OCD126-896901	SNP array	Genotyping	22
nssv15690787	copy number gain	OCD161-RS-1588_1450	SNP array	Genotyping	20
nssv15690912	copy number gain	OCD171-RS-1773	SNP array	Genotyping	19
nssv15693150	copy number gain	OCD86-896851	SNP array	Genotyping	29
nssv15697360	copy number gain	157169	SNP array	Genotyping	13
nssv15699516	copy number gain	155498	SNP array	Genotyping	20
nssv15701981	copy number gain	199597	SNP array	Genotyping	18
nssv15702291	copy number gain	170210	SNP array	Genotyping	18

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv15624454	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15625137	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15627234	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15631715	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15634728	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15638444	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15639490	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15641336	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15641785	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15643047	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15655706	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15669513	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15669536	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15670440	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15674030	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15674333	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15674359	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15674379	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15674803	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15674824	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15674921	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15675470	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15675975	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15676140	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15676427	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15676500	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15677321	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15677381	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15678088	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15678107	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15678474	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15678590	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15678757	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15679508	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15679752	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15680083	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15680355	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15680714	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15681165	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15682146	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15683067	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15687576	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15687979	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15688833	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15688937	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15689136	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15690077	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15690787	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15690912	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15693150	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15697360	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15699516	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15701981	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15702291	Remapped	Good	NC_000014.9:g.(?_2 1935993)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,935,993	22,505,293
nssv15624454	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15625137	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15627234	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15631715	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15634728	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15638444	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15639490	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15641336	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15641785	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15643047	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15655706	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15669513	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15669536	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15670440	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15674030	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15674333	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15674359	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15674379	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15674803	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15674824	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15674921	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15675470	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15675975	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15676140	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15676427	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15676500	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15677321	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15677381	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15678088	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15678107	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15678474	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15678590	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15678757	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15679508	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15679752	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15680083	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15680355	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15680714	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15681165	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15682146	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15683067	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15687576	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15687979	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15688833	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15688937	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280
nssv15689136	Submitted genomic		NC_000014.8:g.(?_2 2404167)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,404,167	22,974,280

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dbVar

Database of genomic structural variation

nsv4365131

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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