A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17423843



Internal ID22481713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:174213252..174215770hg38UCSC Ensembl
chr5:173640255..173642773hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg382519
hg192519
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5890837
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17423843
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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