A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv857727



Internal ID15804997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:55808492..55835816hg38UCSC Ensembl
Innerchr16:55842404..55869728hg19UCSC Ensembl
Innerchr16:54399905..54427229hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3827325
hg1927325
hg1827325
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv572692
Supporting Variants
Samples
Known GenesCES1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv857727
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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