A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149186



Internal ID15527561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:68564104..68890598hg38UCSC Ensembl
Innerchr16:68598007..68924501hg19UCSC Ensembl
Innerchr16:67155508..67482002hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38326495
hg19326495
hg18326495
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv572908
Supporting Variants
SamplesHGDP00512
Known GenesCDH1, CDH3, TANGO6, ZFP90
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149186
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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