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

dbVar

Database of genomic structural variation

nsv5920777

Organism: Homo sapiens

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

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:243

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: 130 SVs from 24 studies. See in: genome view

Submitted genomic105,551,356-105,551,598

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5920777	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	105,551,356	105,551,598
nsv5920777	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	108,313,637	108,313,879

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17433694	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17433694	Submitted genomic		NC_000009.12:g.105 551356_105551598de l	GRCh38 (hg38)		NC_000009.12	Chr9	105,551,356	105,551,598
nssv17433694	Remapped	Perfect	NC_000009.11:g.108 313637_108313879de l	GRCh37.p13	First Pass	NC_000009.11	Chr9	108,313,637	108,313,879

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