A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612560



Internal ID16399969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:139765008..139806792hg38UCSC Ensembl
Innerchr8:140777251..140819035hg19UCSC Ensembl
Innerchr8:140846433..140888217hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3841785
hg1941785
hg1841785
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12366n54
Supporting Variantsnssv1156884
SamplesHGDP00527
Known GenesTRAPPC9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612560
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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