A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568923



Internal ID16356332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:33971817..33989532hg38UCSC Ensembl
Innerchr15:34264018..34281733hg19UCSC Ensembl
Innerchr15:32051310..32069025hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3817716
hg1917716
hg1817716
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149584
SamplesHGDP00328
Known GenesAVEN, CHRM5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568923
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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