A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156886



Internal ID15528589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:140448395..140519958hg38UCSC Ensembl
Innerchr8:141458494..141530057hg19UCSC Ensembl
Innerchr8:141527676..141599239hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3871564
hg1971564
hg1871564
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612566
Supporting Variants
SamplesHGDP00663
Known GenesCHRAC1, TRAPPC9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156886
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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