A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3594161



Internal ID18892442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:73109319..73177882hg38UCSC Ensembl
Innerchr3:73158470..73227033hg19UCSC Ensembl
Innerchr3:73241160..73309723hg18UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3868564
hg1968564
hg1868564
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv998218
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3594161
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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