A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2879891



Internal ID15329779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:219504074..219504458hg38UCSC Ensembl
Innerchr2:220368796..220369180hg19UCSC Ensembl
Innerchr2:220077040..220077424hg18UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38385
hg19385
hg18385
Variant TypeCNV gain
Copy Number14
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514984
Supporting Variants
SamplesNA18555
Known GenesGMPPA
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2879891
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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