A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524418



Internal ID15451711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:31832149..31865293hg38UCSC Ensembl
InnerchrX:31850266..31883410hg19UCSC Ensembl
InnerchrX:31760187..31793331hg18UCSC Ensembl
InnerchrX:31609923..31643067hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3833145
hg1933145
hg1833145
hg1733145
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700344
Samples
Known GenesDMD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524418
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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