A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv856688



Internal ID16150644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:48384822..48385636hg38UCSC Ensembl
Innerchr16:48418733..48419547hg19UCSC Ensembl
Innerchr16:46976234..46977048hg18UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38815
hg19815
hg18815
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv572553
Supporting Variants
Samples
Known GenesMIR548AE2, SIAH1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv856688
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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