A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569807



Internal ID16357216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:68694613..68718290hg38UCSC Ensembl
Innerchr15:68986952..69010629hg19UCSC Ensembl
Innerchr15:66774006..66797683hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3823678
hg1923678
hg1823678
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149236
SamplesHGDP01189
Known GenesCORO2B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569807
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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