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dbVar

Database of genomic structural variation

nsv6047036

Organism: Homo sapiens

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

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

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: 462 SVs from 29 studies. See in: genome view

Submitted genomic141,906,382-141,906,382

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6047036	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000023.11	ChrX	141,906,382	141,906,382
nsv6047036	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000023.10	ChrX	140,994,168	140,994,168

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17649849	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17649849	Submitted genomic		NC_000023.11:g.141 906382_141906383in s141	GRCh38 (hg38)		NC_000023.11	ChrX	141,906,382	141,906,382
nssv17649849	Remapped	Perfect	NC_000023.10:g.140 994168_140994169in s141	GRCh37.p13	First Pass	NC_000023.10	ChrX	140,994,168	140,994,168

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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