A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586495



Internal ID6711191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:153685148..153714589hg38UCSC Ensembl
InnerchrX:152950603..152980044hg19UCSC Ensembl
InnerchrX:152603797..152633238hg18UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3829442
hg1929442
hg1829442
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1003299
Supporting Variants
SamplesHuRef
Known GenesBCAP31, SLC6A8
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586495
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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