A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521798



Internal ID15449091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:32147446..32497512hg38UCSC Ensembl
InnerchrX:32165563..32515629hg19UCSC Ensembl
InnerchrX:32075484..32425550hg18UCSC Ensembl
InnerchrX:31925220..32275286hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38350067
hg19350067
hg18350067
hg17350067
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694568
Samples
Known GenesDMD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521798
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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