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

dbVar

Database of genomic structural variation

nsv5972569

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: 135 SVs from 17 studies. See in: genome view

Submitted genomic42,884,986-42,884,986

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5972569	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000017.11	Chr17	42,884,986	42,884,986
nsv5972569	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000017.10	Chr17	41,037,003	41,037,003

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17371132	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17371132	Submitted genomic		NC_000017.11:g.428 84986_42884987ins5 7	GRCh38 (hg38)		NC_000017.11	Chr17	42,884,986	42,884,986
nssv17371132	Remapped	Perfect	NC_000017.10:g.410 37003_41037004ins5 7	GRCh37.p13	First Pass	NC_000017.10	Chr17	41,037,003	41,037,003

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