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

dbVar

Database of genomic structural variation

nsv5906513

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:2,093

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: 140 SVs from 41 studies. See in: genome view

Submitted genomic102,840,897-102,842,989

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5906513	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000004.12	Chr4	102,840,897	102,842,989
nsv5906513	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000004.11	Chr4	103,762,054	103,764,146

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17428088	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17428088	Submitted genomic		NC_000004.12:g.102 840897_102842989de l	GRCh38 (hg38)		NC_000004.12	Chr4	102,840,897	102,842,989
nssv17428088	Remapped	Perfect	NC_000004.11:g.103 762054_103764146de l	GRCh37.p13	First Pass	NC_000004.11	Chr4	103,762,054	103,764,146

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