A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv508n21



Internal ID22766700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:33047771..33302495hg38UCSC Ensembl
chrX:33065888..33320612hg19UCSC Ensembl
chrX:32975809..33230533hg18UCSC Ensembl
chrX:32825545..33080269hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38254725
hg19254725
hg18254725
hg17254725
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv522469, nsv522100
Samples
Known GenesDMD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv508n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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