A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv843034



Internal ID16136990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:53682370..53684200hg38UCSC Ensembl
Innerchr15:53974567..53976397hg19UCSC Ensembl
Innerchr15:51761859..51763689hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg381831
hg191831
hg181831
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569444
Supporting Variants
Samples
Known GenesWDR72
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv843034
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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