A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv509n21



Internal ID22766701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:33373627..33539786hg38UCSC Ensembl
chrX:33391744..33557903hg19UCSC Ensembl
chrX:33301665..33467824hg18UCSC Ensembl
chrX:33151401..33317560hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38166160
hg19166160
hg18166160
hg17166160
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv526258, nsv516480
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv509n21
Frequency
Sample Size2026
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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