A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526755



Internal ID15454048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:31826331..31845196hg38UCSC Ensembl
InnerchrX:31844448..31863313hg19UCSC Ensembl
InnerchrX:31754369..31773234hg18UCSC Ensembl
InnerchrX:31604105..31622970hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3818866
hg1918866
hg1818866
hg1718866
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703102
Samples
Known GenesDMD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526755
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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