A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565559



Internal ID7036941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:35794033..35804083hg38UCSC Ensembl
Outerchr6:35761810..35771860hg19UCSC Ensembl
Outerchr6:35869788..35879838hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3813238
hg1913238
hg1813238
Variant TypeCNV insertion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv990474
Supporting Variants
SamplesHuRef
Known GenesCLPS
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565559
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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