A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569702



Internal ID16010425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:64702244..64706393hg38UCSC Ensembl
Innerchr15:64994443..64998592hg19UCSC Ensembl
Innerchr15:62781496..62785645hg18UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg384150
hg194150
hg184150
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv843969, nssv843968
Samples
Known GenesOAZ2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569702
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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