A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv857756



Internal ID15805026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:57092244..57093081hg38UCSC Ensembl
Innerchr16:57126156..57126993hg19UCSC Ensembl
Innerchr16:55683657..55684494hg18UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg38838
hg19838
hg18838
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv572705
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)nssv857756
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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