A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569827



Internal ID16357236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71183376..71185709hg38UCSC Ensembl
Innerchr15:71475715..71478048hg19UCSC Ensembl
Innerchr15:69262769..69265102hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg382334
hg192334
hg182334
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4587n54
Supporting Variantsnssv844409, nssv844410, nssv844412, nssv844402, nssv844413, nssv844406, nssv844411, nssv844404, nssv844403, nssv844408, nssv844401, nssv844399, nssv844407, nssv844414, nssv844400, nssv844405
Samples
Known GenesTHSD4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569827
Frequency
Sample Size17421
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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