A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522637



Internal ID15449930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:32719542..32796071hg38UCSC Ensembl
InnerchrX:32737659..32814188hg19UCSC Ensembl
InnerchrX:32647580..32724109hg18UCSC Ensembl
InnerchrX:32497316..32573845hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3876530
hg1976530
hg1876530
hg1776530
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv507n21
Supporting Variantsnssv706035
Samples
Known GenesDMD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522637
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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