A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033827



Internal ID19123048
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 StatusM
Merged Variantsdgv5626n100
Supporting Variantsnssv3637055
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)nsv1033827
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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