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

dbVar

Database of genomic structural variation

nsv5925518

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:306

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

Submitted genomic62,780,684-62,780,989

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5925518	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	62,780,684	62,780,989
nsv5925518	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	62,548,156	62,548,461

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17361797	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17361797	Submitted genomic		NC_000011.10:g.627 80684_62780989del	GRCh38 (hg38)		NC_000011.10	Chr11	62,780,684	62,780,989
nssv17361797	Remapped	Perfect	NC_000011.9:g.6254 8156_62548461del	GRCh37.p13	First Pass	NC_000011.9	Chr11	62,548,156	62,548,461

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