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

dbVar

Database of genomic structural variation

nsv5911485

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:6,116

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: 119 SVs from 29 studies. See in: genome view

Submitted genomic63,348,549-63,354,664

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5911485	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	63,348,549	63,354,664
nsv5911485	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	65,108,309	65,114,424

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17356813	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17356813	Submitted genomic		NC_000010.11:g.633 48549_63354664del	GRCh38 (hg38)		NC_000010.11	Chr10	63,348,549	63,354,664
nssv17356813	Remapped	Perfect	NC_000010.10:g.651 08309_65114424del	GRCh37.p13	First Pass	NC_000010.10	Chr10	65,108,309	65,114,424

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