A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3637055



Internal ID18935336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:34055915..34187597hg38UCSC Ensembl
Innerchr5:34056020..34187702hg19UCSC Ensembl
Innerchr5:34091777..34223459hg18UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38131683
hg19131683
hg18131683
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033827
Supporting Variants
Samples
Known GenesC1QTNF3-AMACR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3637055
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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