Warning: The NCBI web site requires JavaScript to function. more...

dbVar

Database of genomic structural variation

nsv4650693

Organism: Homo sapiens

Study:nstd186 (NCBI Curated Common Structural Variants)
Variant Type:copy number variation
Method Type:Curated
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:263

Description:nsv4250046 from gnomAD Structural Variants. For a full list of variants now included in nstd186, refer to the mapping file provided here.

Links to Other Resources

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

Remapped(Score: Perfect):89,325,084-89,325,346

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4650693	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000015.10	Chr15	89,325,084	89,325,346
nsv4650693	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000015.9	Chr15	89,868,315	89,868,577

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16171622	deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16171622	Remapped	Perfect	NC_000015.10:g.893 25084_89325346del	GRCh38.p12	First Pass	NC_000015.10	Chr15	89,325,084	89,325,346
nssv16171622	Submitted genomic		NC_000015.9:g.8986 8315_89868577del	GRCh37 (hg19)		NC_000015.9	Chr15	89,868,315	89,868,577

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv16171622	0.197	4272	21670

You are here: NCBI