A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586765



Internal ID6711461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:54626656..54629840hg38UCSC Ensembl
Innerchr1:55092329..55095513hg19UCSC Ensembl
Innerchr1:54864917..54868101hg18UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg383185
hg193185
hg183185
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1004742
Supporting Variants
SamplesHuRef
Known GenesACOT11
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586765
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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