A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv863332



Internal ID15810602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89390106..89421643hg38UCSC Ensembl
Innerchr16:89456514..89488051hg19UCSC Ensembl
Innerchr16:87984015..88015552hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3831538
hg1931538
hg1831538
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573736
Supporting Variants
Samples
Known GenesANKRD11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv863332
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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