A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv520n21



Internal ID22766712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:96817047..97148876hg38UCSC Ensembl
chrX:96072046..96403875hg19UCSC Ensembl
chrX:95958702..96290531hg18UCSC Ensembl
chrX:95878191..96210020hg17UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38331830
hg19331830
hg18331830
hg17331830
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv515760, nsv521409
Samples
Known GenesDIAPH2, RPA4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv520n21
Frequency
Sample Size2026
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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