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

dbVar

Database of genomic structural variation

nsv5968517

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: 82 SVs from 20 studies. See in: genome view

Submitted genomic80,206,449-80,206,449

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5968517	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000014.9	Chr14	80,206,449	80,206,449
nsv5968517	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000014.8	Chr14	80,672,792	80,672,792

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17378335	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17378335	Submitted genomic		NC_000014.9:g.8020 6449_80206450ins30 9	GRCh38 (hg38)		NC_000014.9	Chr14	80,206,449	80,206,449
nssv17378335	Remapped	Perfect	NC_000014.8:g.8067 2792_80672793ins30 9	GRCh37.p13	First Pass	NC_000014.8	Chr14	80,672,792	80,672,792

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