A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614582



Internal ID16401991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:70143826..70148520hg38UCSC Ensembl
Innerchr9:72758742..72763436hg19UCSC Ensembl
Innerchr9:71948562..71953256hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg384695
hg194695
hg184695
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1137122
Samples
Known GenesMAMDC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614582
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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