A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569704



Internal ID16010427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:65162973..65178902hg38UCSC Ensembl
Innerchr15:65455311..65471240hg19UCSC Ensembl
Innerchr15:63242364..63258293hg18UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3815930
hg1915930
hg1815930
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv843971
Samples
Known GenesCLPX
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569704
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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