A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610546



Internal ID16397955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:15545427..15562617hg38UCSC Ensembl
Innerchr8:15402936..15420126hg19UCSC Ensembl
Innerchr8:15447307..15464497hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3817191
hg1917191
hg1817191
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12017n54
Supporting Variantsnssv1156320
SamplesHGDP00805
Known GenesTUSC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610546
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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