A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604437



Internal ID16391846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:105137636..105213575hg38UCSC Ensembl
Innerchr6:105585511..105661450hg19UCSC Ensembl
Innerchr6:105692204..105768143hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3875940
hg1975940
hg1875940
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1071886
Samples
Known GenesBVES-AS1, POPDC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604437
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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