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dbVar

Database of genomic structural variation

nsv6101181

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:542

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: 304 SVs from 48 studies. See in: genome view

Submitted genomic26,001,844-26,002,385

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6101181	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000021.9	Chr21	26,001,844	26,002,385
nsv6101181	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000021.8	Chr21	27,374,159	27,374,700

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17649817	inversion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17649817	Submitted genomic		NC_000021.9:g.2600 1844_26002385inv	GRCh38 (hg38)		NC_000021.9	Chr21	26,001,844	26,002,385
nssv17649817	Remapped	Perfect	NC_000021.8:g.2737 4159_27374700inv	GRCh37.p13	First Pass	NC_000021.8	Chr21	27,374,159	27,374,700

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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