A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586292



Internal ID7057674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:39360357..39360868hg38UCSC Ensembl
Innerchr13:39934494..39935005hg19UCSC Ensembl
Innerchr13:38832494..38833005hg18UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38512
hg19512
hg18512
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv995533
Supporting Variants
SamplesHuRef
Known GenesLHFP
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586292
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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