A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv501n21



Internal ID20132222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:14115921..14251716hg38UCSC Ensembl
chrX:14134040..14269838hg19UCSC Ensembl
chrX:14043961..14179759hg18UCSC Ensembl
chrX:13893697..14029495hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38135796
hg19135799
hg18135799
hg17135799
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv528086, nsv528363, nsv527337
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv501n21
Frequency
Sample Size2026
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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