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dbVar

Database of genomic structural variation

nsv4240750

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:6,738

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: 77 SVs from 13 studies. See in: genome view

Remapped(Score: Perfect):74,907,671-74,914,408

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4240750	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000015.10	Chr15	74,907,671	74,914,408
nsv4240750	Submitted genomic		GRCh37.p13	Primary Assembly		NC_000015.9	Chr15	75,200,012	75,206,749

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15826197	deletion	Sequencing	Other

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv15826197	Remapped	Perfect	NC_000015.10:g.749 07671_74914408del	GRCh38.p12	First Pass	NC_000015.10	Chr15	74,907,671	74,914,408
nssv15826197	Submitted genomic		NC_000015.9:g.7520 0012_75206749del	GRCh37.p13		NC_000015.9	Chr15	75,200,012	75,206,749

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)
nssv15826197	5e-005	1	20044

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