A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565377



Internal ID7036759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:170202994..170205970hg38UCSC Ensembl
Outerchr5:169629998..169632974hg19UCSC Ensembl
Outerchr5:169562576..169565552hg18UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg385147
hg195147
hg185147
Variant TypeCNV insertion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1007904
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565377
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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