A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569828



Internal ID16357237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71183376..71186817hg38UCSC Ensembl
Innerchr15:71475715..71479156hg19UCSC Ensembl
Innerchr15:69262769..69266210hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg383442
hg193442
hg183442
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4588n54
Supporting Variantsnssv844415, nssv844418, nssv844419, nssv844417, nssv844420, nssv844416
Samples
Known GenesTHSD4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569828
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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