A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522116



Internal ID15449409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:5205985..5350397hg38UCSC Ensembl
InnerchrX:5124026..5268438hg19UCSC Ensembl
InnerchrX:5134026..5278438hg18UCSC Ensembl
InnerchrX:4983762..5128174hg17UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg38144413
hg19144413
hg18144413
hg17144413
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694889
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522116
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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