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

dbVar

Database of genomic structural variation

nsv6108580

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: 126 SVs from 21 studies. See in: genome view

Submitted genomic35,886,758-35,886,758

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6108580	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	35,886,758	35,886,758
nsv6108580	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	36,377,660	36,377,660

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17632299	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17632299	Submitted genomic		NC_000019.10:g.358 86758_35886759ins5 3	GRCh38 (hg38)		NC_000019.10	Chr19	35,886,758	35,886,758
nssv17632299	Remapped	Perfect	NC_000019.9:g.3637 7660_36377661ins53	GRCh37.p13	First Pass	NC_000019.9	Chr19	36,377,660	36,377,660

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