A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv510n21



Internal ID11601188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:38257469..38318714hg38UCSC Ensembl
chrX:38116722..38177967hg19UCSC Ensembl
chrX:38001666..38062911hg18UCSC Ensembl
chrX:37872939..37934184hg17UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg3861246
hg1961246
hg1861246
hg1761246
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv520388, nsv520298
Samples
Known GenesRPGR
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv510n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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