A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524221



Internal ID15104828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:5844994..5879843hg38UCSC Ensembl
InnerchrX:5763035..5797884hg19UCSC Ensembl
InnerchrX:5773035..5807884hg18UCSC Ensembl
InnerchrX:5622771..5657620hg17UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg3834850
hg1934850
hg1834850
hg1734850
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700109
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524221
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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