A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586434



Internal ID6711130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:7216639..7222754hg38UCSC Ensembl
Innerchr4:7218366..7224481hg19UCSC Ensembl
Innerchr4:7269267..7275382hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg386116
hg196116
hg186116
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv993203
Supporting Variants
SamplesHuRef
Known GenesSORCS2
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586434
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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