A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519609



Internal ID15446902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:31282045..31303977hg38UCSC Ensembl
InnerchrX:31300162..31322094hg19UCSC Ensembl
InnerchrX:31210083..31232015hg18UCSC Ensembl
InnerchrX:31059819..31081751hg17UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg3821933
hg1921933
hg1821933
hg1721933
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694337
Samples
Known GenesDMD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519609
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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