A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv843038



Internal ID16136994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:53682798..53684200hg38UCSC Ensembl
Innerchr15:53974995..53976397hg19UCSC Ensembl
Innerchr15:51762287..51763689hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg381403
hg191403
hg181403
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569447
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)nssv843038
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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