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dbVar

Database of genomic structural variation

nsv5671538

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:inversion
Method Type:Optical mapping, Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:438

Publication(s):Ebert et al. 2021

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: 224 SVs from 32 studies. See in: genome view

Submitted genomic97,456,278-97,456,715

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5671538	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000013.11	Chr13	97,456,278	97,456,715
nsv5671538	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000013.10	Chr13	98,108,532	98,108,969

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17095818	inversion	Optical mapping, Sequencing	Optical mapping, Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17095818	Submitted genomic		NC_000013.11:g.974 56278_97456715inv	GRCh38 (hg38)		NC_000013.11	Chr13	97,456,278	97,456,715
nssv17095818	Remapped	Perfect	NC_000013.10:g.981 08532_98108969inv	GRCh37.p13	First Pass	NC_000013.10	Chr13	98,108,532	98,108,969

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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