A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525738



Internal ID15453031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:33277057..33349242hg38UCSC Ensembl
InnerchrX:33295174..33367359hg19UCSC Ensembl
InnerchrX:33205095..33277280hg18UCSC Ensembl
InnerchrX:33054831..33127016hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3872186
hg1972186
hg1872186
hg1772186
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701903
Samples
Known GenesDMD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525738
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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