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dbVar

Database of genomic structural variation

nsv4871044

Organism: Homo sapiens

Study:nstd200 (Abel et al. 2020)
Variant Type:inversion
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:49,082,546

Publication(s):Abel et al. 2020

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: 134334 SVs from 144 studies. See in: genome view

Remapped(Score: Good):63,639,797-112,722,344

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4871044	Remapped	Good	GRCh38.p12	Primary Assembly	First Pass	NC_000013.11	Chr13	63,639,798 (-1, +1)	112,722,343 (+1)
nsv4871044	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000013.10	Chr13	64,213,931 (-1, +1)	113,376,657 (+1)

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16409743	inversion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16409743	Remapped	Good	NC_000013.11:g.(63 639797_63639799)_( ?_112722344)inv	GRCh38.p12	First Pass	NC_000013.11	Chr13	63,639,798 (-1, +1)	112,722,343 (+1)
nssv16409743	Submitted genomic		NC_000013.10:g.(64 213930_64213932)_( ?_113376658)inv	GRCh37 (hg19)		NC_000013.10	Chr13	64,213,931 (-1, +1)	113,376,657 (+1)

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)
nssv16409743	<0.001	1	16834

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