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dbVar

Database of genomic structural variation

nsv6109150

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:57,549

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: 243 SVs from 43 studies. See in: genome view

Submitted genomic88,757,023-88,814,571

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6109150	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	88,757,023	88,814,571
nsv6109150	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	88,490,191	88,547,739

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17578005	inversion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17578005	Submitted genomic		NC_000011.10:g.887 57023_88814571inv	GRCh38 (hg38)		NC_000011.10	Chr11	88,757,023	88,814,571
nssv17578005	Remapped	Perfect	NC_000011.9:g.8849 0191_88547739inv	GRCh37.p13	First Pass	NC_000011.9	Chr11	88,490,191	88,547,739

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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