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dbVar

Database of genomic structural variation

nsv4172145

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:119

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: 42 SVs from 11 studies. See in: genome view

Remapped(Score: Perfect):65,399,116-65,399,234

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4172145	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000008.11	Chr8	65,399,116	65,399,234
nsv4172145	Submitted genomic		GRCh37.p13	Primary Assembly		NC_000008.10	Chr8	66,311,351	66,311,469

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15926432	deletion	Sequencing	Other

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv15926432	Remapped	Perfect	NC_000008.11:g.653 99116_65399234del	GRCh38.p12	First Pass	NC_000008.11	Chr8	65,399,116	65,399,234
nssv15926432	Submitted genomic		NC_000008.10:g.663 11351_66311469del	GRCh37.p13		NC_000008.10	Chr8	66,311,351	66,311,469

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)
nssv15926432	0.324	7022	21694

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