A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv518n21



Internal ID22766710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:88230705..88372009hg38UCSC Ensembl
chrX:87485706..87627010hg19UCSC Ensembl
chrX:87372362..87513666hg18UCSC Ensembl
chrX:87291851..87433155hg17UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg38141305
hg19141305
hg18141305
hg17141305
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv523682, nsv518355
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv518n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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