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dbVar

Database of genomic structural variation

nsv4284096

Organism: Homo sapiens

Study:nstd166 (gnomAD Structural Variants)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:463

Publication(s):gnomAD_Structural_Variants

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: 38 SVs from 6 studies. See in: genome view

Remapped(Score: Perfect):59,931,590-59,932,052

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4284096	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000020.11	Chr20	59,931,590	59,932,052
nsv4284096	Submitted genomic		GRCh37.p13	Primary Assembly		NC_000020.10	Chr20	58,506,645	58,507,107

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15862500	deletion	Sequencing	Other

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv15862500	Remapped	Perfect	NC_000020.11:g.599 31590_59932052del	GRCh38.p12	First Pass	NC_000020.11	Chr20	59,931,590	59,932,052
nssv15862500	Submitted genomic		NC_000020.10:g.585 06645_58507107del	GRCh37.p13		NC_000020.10	Chr20	58,506,645	58,507,107

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv15862500	4.6e-005	1	21694

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