A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524503



Internal ID15105110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:126044730..126316838hg38UCSC Ensembl
InnerchrX:125178713..125450821hg19UCSC Ensembl
InnerchrX:125006394..125278502hg18UCSC Ensembl
InnerchrX:124904248..125176356hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38272109
hg19272109
hg18272109
hg17272109
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700447
Samples
Known GenesDCAF12L2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524503
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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