A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv503n21



Internal ID20132224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:17329494..17542854hg38UCSC Ensembl
chrX:17347617..17560976hg19UCSC Ensembl
chrX:17257538..17470897hg18UCSC Ensembl
chrX:17107274..17320633hg17UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg38213361
hg19213360
hg18213360
hg17213360
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv528560, nsv522285
Samples
Known GenesMIR4768, NHS
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv503n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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