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dbVar

Database of genomic structural variation

nsv4116602

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:381,145

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: 587 SVs from 19 studies. See in: genome view

Remapped(Score: Perfect):19,071,919-19,453,063

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4116602	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000005.10	Chr5	19,071,919	19,453,063
nsv4116602	Submitted genomic		GRCh37.p13	Primary Assembly		NC_000005.9	Chr5	19,072,028	19,453,172

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15899991	deletion	Sequencing	Other

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv15899991	Remapped	Perfect	NC_000005.10:g.190 71919_19453063del	GRCh38.p12	First Pass	NC_000005.10	Chr5	19,071,919	19,453,063
nssv15899991	Submitted genomic		NC_000005.9:g.1907 2028_19453172del	GRCh37.p13		NC_000005.9	Chr5	19,072,028	19,453,172

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)
nssv15899991	9.2e-005	2	21694

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