A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv533n21



Internal ID22766725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:140804585..140844602hg38UCSC Ensembl
chrX:139886750..139926767hg19UCSC Ensembl
chrX:139714416..139754433hg18UCSC Ensembl
chrX:139612270..139652287hg17UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg3840018
hg1940018
hg1840018
hg1740018
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv527132, nsv517824
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv533n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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