A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525602



Internal ID15452895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:32835148..32840909hg38UCSC Ensembl
InnerchrX:32853265..32859026hg19UCSC Ensembl
InnerchrX:32763186..32768947hg18UCSC Ensembl
InnerchrX:32612922..32618683hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg385762
hg195762
hg185762
hg175762
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701746
Samples
Known GenesDMD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525602
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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