A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517938



Internal ID15098545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:15296656..15331048hg38UCSC Ensembl
InnerchrX:15314778..15349170hg19UCSC Ensembl
InnerchrX:15224699..15259091hg18UCSC Ensembl
InnerchrX:15074435..15108827hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3834393
hg1934393
hg1834393
hg1734393
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695350
Samples
Known GenesASB11, PIGA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517938
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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