Warning: The NCBI web site requires JavaScript to function. more...

dbVar

Database of genomic structural variation

nsv6047062

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: 119 SVs from 22 studies. See in: genome view

Submitted genomic93,876,095-93,876,095

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6047062	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	93,876,095	93,876,095
nsv6047062	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	94,341,651	94,341,651

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17531606	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17531606	Submitted genomic		NC_000001.11:g.938 76095_93876096ins4 74	GRCh38 (hg38)		NC_000001.11	Chr1	93,876,095	93,876,095
nssv17531606	Remapped	Perfect	NC_000001.10:g.943 41651_94341652ins4 74	GRCh37.p13	First Pass	NC_000001.10	Chr1	94,341,651	94,341,651

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.

You are here: NCBI