A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523241



Internal ID15103848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:32594177..32625336hg38UCSC Ensembl
InnerchrX:32612294..32643453hg19UCSC Ensembl
InnerchrX:32522215..32553374hg18UCSC Ensembl
InnerchrX:32371951..32403110hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3831160
hg1931160
hg1831160
hg1731160
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698969
Samples
Known GenesDMD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523241
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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