A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2982014



Internal ID15769251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:149804877..149899945hg38UCSC Ensembl
InnerchrX:148886539..149028718hg19UCSC Ensembl
InnerchrX:148694336..148789376hg18UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3895069
hg19142180
hg1895041
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515182
Supporting Variants
SamplesNA19237
Known GenesMAGEA8, MAGEA8-AS1
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2982014
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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