A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520298



Internal ID15100905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:38263654..38318714hg38UCSC Ensembl
InnerchrX:38122907..38177967hg19UCSC Ensembl
InnerchrX:38007851..38062911hg18UCSC Ensembl
InnerchrX:37879124..37934184hg17UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg3855061
hg1955061
hg1855061
hg1755061
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv510n21
Supporting Variantsnssv697334
Samples
Known GenesRPGR
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520298
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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