A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586579



Internal ID7057961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:119900852..119924377hg38UCSC Ensembl
InnerchrX:119034815..119058340hg19UCSC Ensembl
InnerchrX:118918843..118942368hg18UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3823526
hg1923526
hg1823526
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv989689
Supporting Variants
SamplesHuRef
Known GenesAKAP14
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586579
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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