A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv41e209



Internal ID20126431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:119900037..119924413hg38UCSC Ensembl
chrX:119034000..119058376hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3824377
hg1924377
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2990457, esv2854014
SamplesHuRef
Known GenesAKAP14
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)dgv41e209
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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