A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv863331



Internal ID15810601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89307299..89446826hg38UCSC Ensembl
Innerchr16:89373707..89513234hg19UCSC Ensembl
Innerchr16:87901208..88040735hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38139528
hg19139528
hg18139528
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573735
Supporting Variants
Samples
Known GenesANKRD11, LOC100287036
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv863331
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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