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dbVar

Database of genomic structural variation

nsv6102457

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:191,106

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: 452 SVs from 56 studies. See in: genome view

Submitted genomic79,260,363-79,451,468

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6102457	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	79,260,363	79,451,468
nsv6102457	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	79,487,489	79,678,594

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17533850	inversion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17533850	Submitted genomic		NC_000002.12:g.792 60363_79451468inv	GRCh38 (hg38)		NC_000002.12	Chr2	79,260,363	79,451,468
nssv17533850	Remapped	Perfect	NC_000002.11:g.794 87489_79678594inv	GRCh37.p13	First Pass	NC_000002.11	Chr2	79,487,489	79,678,594

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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