A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569701



Internal ID16010424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:64700971..64702760hg38UCSC Ensembl
Innerchr15:64993170..64994959hg19UCSC Ensembl
Innerchr15:62780223..62782012hg18UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg381790
hg191790
hg181790
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv843967
Samples
Known GenesOAZ2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569701
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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