A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv530n21



Internal ID22766722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:127481933..127564723hg38UCSC Ensembl
chrX:126615914..126698704hg19UCSC Ensembl
chrX:126443595..126526385hg18UCSC Ensembl
chrX:126341449..126424239hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3882791
hg1982791
hg1882791
hg1782791
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv524356, nsv527964
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv530n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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