A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv499n21



Internal ID20132220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:7777235..8383635hg38UCSC Ensembl
chrX:7745276..8351676hg19UCSC Ensembl
chrX:7705276..8311676hg18UCSC Ensembl
chrX:7555012..8161412hg17UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38606401
hg19606401
hg18606401
hg17606401
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv518656, nsv518551
Samples
Known GenesMIR651, PNPLA4, VCX, VCX2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv499n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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