A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612561



Internal ID16399970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:139765008..139810722hg38UCSC Ensembl
Innerchr8:140777251..140822965hg19UCSC Ensembl
Innerchr8:140846433..140892147hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3845715
hg1945715
hg1845715
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12366n54
Supporting Variantsnssv1156885
SamplesNINDS_111
Known GenesTRAPPC9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612561
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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