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dbVar

Database of genomic structural variation

nsv4219280

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:8,001

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

Remapped(Score: Perfect):22,915,791-22,923,791

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4219280	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000014.9	Chr14	22,915,791	22,923,791
nsv4219280	Submitted genomic		GRCh37.p13	Primary Assembly		NC_000014.8	Chr14	23,385,000	23,393,000

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15950879	duplication	Sequencing	Other

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv15950879	Remapped	Perfect	NC_000014.9:g.2291 5791_22923791dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	22,915,791	22,923,791
nssv15950879	Submitted genomic		NC_000014.8:g.2338 5000_23393000dup	GRCh37.p13		NC_000014.8	Chr14	23,385,000	23,393,000

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)
nssv15950879	0.005	96	21320

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