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

dbVar

Database of genomic structural variation

nsv5970075

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

Submitted genomic51,698,793-51,698,793

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5970075	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000015.10	Chr15	51,698,793	51,698,793
nsv5970075	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	51,990,990	51,990,990

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17385533	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17385533	Submitted genomic		NC_000015.10:g.516 98793_51698794ins3 25	GRCh38 (hg38)		NC_000015.10	Chr15	51,698,793	51,698,793
nssv17385533	Remapped	Perfect	NC_000015.9:g.5199 0990_51990991ins32 5	GRCh37.p13	First Pass	NC_000015.9	Chr15	51,990,990	51,990,990

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