A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17547519



Internal ID21871874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:37361137..37362233hg38UCSC Ensembl
chr3:37402628..37403724hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg381097
hg191097
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5993823
Supporting Variants
Samples
Known GenesGOLGA4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17547519
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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