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dbVar

Database of genomic structural variation

nsv4718858

Organism: Homo sapiens

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

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

Description:nsv4547272 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: 91 SVs from 24 studies. See in: genome view

Remapped(Score: Perfect):50,726,245-50,726,245

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4718858	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000016.10	Chr16	50,726,245	50,726,245
nsv4718858	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000016.9	Chr16	50,760,156	50,760,156

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16228257	insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16228257	Remapped	Perfect	NC_000016.10:g.507 26245_50726246ins?	GRCh38.p12	First Pass	NC_000016.10	Chr16	50,726,245	50,726,245
nssv16228257	Submitted genomic		NC_000016.9:g.5076 0156_50760157ins?	GRCh37 (hg19)		NC_000016.9	Chr16	50,760,156	50,760,156

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)
nssv16228257	0.02	423	21670

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