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dbVar

Database of genomic structural variation

nsv6133895

Organism: Homo sapiens

Study:nstd213 (Pham et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:33,099

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: 906 SVs from 79 studies. See in: genome view

Remapped(Score: Perfect):1,580,434-1,613,532

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nsv6133895	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000020.11	Chr20	1,580,434	1,580,443	1,613,524	1,613,532
nsv6133895	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000020.10	Chr20	1,561,080	1,561,089	1,594,170	1,594,178

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17679004	deletion	SAMN20524659	Sequencing	Paired-end mapping	203

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nssv17679004	Remapped	Perfect	NC_000020.11:g.(15 80434_1580443)_(16 13524_1613532)del	GRCh38.p12	First Pass	NC_000020.11	Chr20	1,580,434	1,580,443	1,613,524	1,613,532
nssv17679004	Submitted genomic		NC_000020.10:g.(15 61080_1561089)_(15 94170_1594178)del	GRCh37 (hg19)		NC_000020.10	Chr20	1,561,080	1,561,089	1,594,170	1,594,178

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

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