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

dbVar

Database of genomic structural variation

nsv6094991

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: 130 SVs from 23 studies. See in: genome view

Submitted genomic30,806,775-30,806,775

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6094991	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000013.11	Chr13	30,806,775	30,806,775
nsv6094991	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000013.10	Chr13	31,380,912	31,380,912

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17610738	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17610738	Submitted genomic		NC_000013.11:g.308 06775_30806776ins5 4	GRCh38 (hg38)		NC_000013.11	Chr13	30,806,775	30,806,775
nssv17610738	Remapped	Perfect	NC_000013.10:g.313 80912_31380913ins5 4	GRCh37.p13	First Pass	NC_000013.10	Chr13	31,380,912	31,380,912

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