A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528125



Internal ID15455418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:33676296..33711285hg38UCSC Ensembl
InnerchrX:33694413..33729402hg19UCSC Ensembl
InnerchrX:33604334..33639323hg18UCSC Ensembl
InnerchrX:33454070..33489059hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3834990
hg1934990
hg1834990
hg1734990
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704670
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528125
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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