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

dbVar

Database of genomic structural variation

nsv5980344

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

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

Publication(s):Almarri et al. 2020

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: 177 SVs from 33 studies. See in: genome view

Submitted genomic84,626,847-84,626,847

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5980344	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	84,626,847	84,626,847
nsv5980344	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	84,337,890	84,337,890

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17368008	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17368008	Submitted genomic		NC_000011.10:g.846 26847_84626848ins5 8	GRCh38 (hg38)		NC_000011.10	Chr11	84,626,847	84,626,847
nssv17368008	Remapped	Perfect	NC_000011.9:g.8433 7890_84337891ins58	GRCh37.p13	First Pass	NC_000011.9	Chr11	84,337,890	84,337,890

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