A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv536n21



Internal ID22766728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:145221633..145237657hg38UCSC Ensembl
chrX:144303153..144319177hg19UCSC Ensembl
chrX:144110845..144126869hg18UCSC Ensembl
chrX:144008699..144024723hg17UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg3816025
hg1916025
hg1816025
hg1716025
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv521264, nsv524712
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv536n21
Frequency
Sample Size2026
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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