A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569835



Internal ID16357244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71183826..71185709hg38UCSC Ensembl
Innerchr15:71476165..71478048hg19UCSC Ensembl
Innerchr15:69263219..69265102hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381884
hg191884
hg181884
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4590n54
Supporting Variantsnssv844437, nssv844439, nssv844441, nssv844435, nssv844440, nssv844438, nssv844442, nssv844436, nssv844434
Samples
Known GenesTHSD4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569835
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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