A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv521n21



Internal ID22766713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:98559306..98683088hg38UCSC Ensembl
chrX:97814304..97938086hg19UCSC Ensembl
chrX:97700960..97824742hg18UCSC Ensembl
chrX:97620449..97744231hg17UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38123783
hg19123783
hg18123783
hg17123783
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv517679, nsv525519, nsv526259
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv521n21
Frequency
Sample Size2026
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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