A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv498n21



Internal ID22766690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:4800596..4933015hg38UCSC Ensembl
chrX:4718637..4851056hg19UCSC Ensembl
chrX:4728637..4861056hg18UCSC Ensembl
chrX:4578373..4710792hg17UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg38132420
hg19132420
hg18132420
hg17132420
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv525973, nsv527698
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv498n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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