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dbVar

Database of genomic structural variation

nsv6108315

Organism: Homo sapiens

Study:nstd212 (Wu et al. 2021)
Variant Type:inversion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:38,779

Publication(s):Wu 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: 431 SVs from 61 studies. See in: genome view

Submitted genomic87,123,269-87,162,047

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6108315	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	87,123,269	87,162,047
nsv6108315	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	87,350,392	87,389,170

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17529619	inversion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17529619	Submitted genomic		NC_000002.12:g.871 23269_87162047inv	GRCh38 (hg38)		NC_000002.12	Chr2	87,123,269	87,162,047
nssv17529619	Remapped	Perfect	NC_000002.11:g.873 50392_87389170inv	GRCh37.p13	First Pass	NC_000002.11	Chr2	87,350,392	87,389,170

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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