A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv859073



Internal ID15806343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:67790492..67807226hg38UCSC Ensembl
Innerchr16:67824395..67841129hg19UCSC Ensembl
Innerchr16:66381896..66398630hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3816735
hg1916735
hg1816735
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv572907
Supporting Variants
Samples
Known GenesRANBP10, TSNAXIP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv859073
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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