A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2982002



Internal ID15758638
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 loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515182
Supporting Variants
SamplesNA19194
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)nssv2982002
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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