A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520240



Internal ID15100847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:23397772..23464530hg38UCSC Ensembl
InnerchrX:23415889..23482647hg19UCSC Ensembl
InnerchrX:23325810..23392568hg18UCSC Ensembl
InnerchrX:23175546..23242304hg17UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3866759
hg1966759
hg1866759
hg1766759
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697302
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520240
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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