A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2832168



Internal ID15280038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:45514695..45520131hg38UCSC Ensembl
Innerchr17:43592061..43597497hg19UCSC Ensembl
Innerchr17:40947844..40953280hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg385437
hg195437
hg185437
Variant TypeCNV gain
Copy Number34
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514848
Supporting Variants
SamplesNA12264
Known GenesLRRC37A4P
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2832168
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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