A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612966



Internal ID16053689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:144532947..144545017hg38UCSC Ensembl
Innerchr8:145758331..145770401hg19UCSC Ensembl
Innerchr8:145729139..145741209hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3812071
hg1912071
hg1812071
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12444n54
Supporting Variantsnssv1125829
Samples
Known GenesARHGAP39
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612966
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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