A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv857741



Internal ID16151697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:57092192..57093132hg38UCSC Ensembl
Innerchr16:57126104..57127044hg19UCSC Ensembl
Innerchr16:55683605..55684545hg18UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg38941
hg19941
hg18941
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv572701
Supporting Variants
Samples
Known GenesCPNE2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv857741
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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