A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569895



Internal ID16357304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71589459..71597728hg38UCSC Ensembl
Innerchr15:71881798..71890067hg19UCSC Ensembl
Innerchr15:69668852..69677121hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg388270
hg198270
hg188270
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv844857
Samples
Known GenesTHSD4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569895
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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