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dbVar

Database of genomic structural variation

nsv4724205

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:nsv4539018 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: 107 SVs from 21 studies. See in: genome view

Remapped(Score: Perfect):95,222,837-95,222,837

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4724205	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000010.11	Chr10	95,222,837	95,222,837
nsv4724205	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000010.10	Chr10	96,982,594	96,982,594

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16217029	insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16217029	Remapped	Perfect	NC_000010.11:g.952 22837_95222838ins?	GRCh38.p12	First Pass	NC_000010.11	Chr10	95,222,837	95,222,837
nssv16217029	Submitted genomic		NC_000010.10:g.969 82594_96982595ins?	GRCh37 (hg19)		NC_000010.10	Chr10	96,982,594	96,982,594

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)
nssv16217029	0.05	1078	21554

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