A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527706



Internal ID15454999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:33191063..33252334hg38UCSC Ensembl
InnerchrX:33209180..33270451hg19UCSC Ensembl
InnerchrX:33119101..33180372hg18UCSC Ensembl
InnerchrX:32968837..33030108hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3861272
hg1961272
hg1861272
hg1761272
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704185
Samples
Known GenesDMD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527706
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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