A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519221



Internal ID15446514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:115942186..115993420hg38UCSC Ensembl
InnerchrX:115058519..115109753hg19UCSC Ensembl
InnerchrX:114972547..115023781hg18UCSC Ensembl
InnerchrX:114870401..114921635hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3851235
hg1951235
hg1851235
hg1751235
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696711
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519221
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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