A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2995008



Internal ID15772453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:95760801..95891793hg38UCSC Ensembl
InnerchrX:95015800..95146792hg19UCSC Ensembl
InnerchrX:94902456..95033448hg18UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38130993
hg19130993
hg18130993
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515224
Supporting Variants
SamplesNA19252
Known GenesMIR548AE1
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2995008
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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