A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518609



Internal ID15445902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:4947777..4985030hg38UCSC Ensembl
InnerchrX:4865818..4903071hg19UCSC Ensembl
InnerchrX:4875818..4913071hg18UCSC Ensembl
InnerchrX:4725554..4762807hg17UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg3837254
hg1937254
hg1837254
hg1737254
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696056
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518609
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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