A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3593774



Internal ID18545369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46760315..46836636hg38UCSC Ensembl
Innerchr3:46801805..46878126hg19UCSC Ensembl
Innerchr3:46776809..46853130hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3876322
hg1976322
hg1876322
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1000774
Supporting Variants
Samples
Known GenesPRSS42
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3593774
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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