A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518902



Internal ID15446195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:39785884..39802914hg38UCSC Ensembl
InnerchrX:39645138..39662168hg19UCSC Ensembl
InnerchrX:39530082..39547112hg18UCSC Ensembl
InnerchrX:39401362..39418392hg17UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg3817031
hg1917031
hg1817031
hg1717031
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv511n21
Supporting Variantsnssv696360
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518902
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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