A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526588



Internal ID15453881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:32545146..32578400hg38UCSC Ensembl
InnerchrX:32563263..32596517hg19UCSC Ensembl
InnerchrX:32473184..32506438hg18UCSC Ensembl
InnerchrX:32322920..32356174hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3833255
hg1933255
hg1833255
hg1733255
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702906
Samples
Known GenesDMD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526588
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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