A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv529n21



Internal ID22766721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:121583547..121820265hg38UCSC Ensembl
chrX:120717401..120954118hg19UCSC Ensembl
chrX:120545082..120781799hg18UCSC Ensembl
chrX:120442936..120679653hg17UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38236719
hg19236718
hg18236718
hg17236718
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv520535, nsv525038
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv529n21
Frequency
Sample Size2026
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer