A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3563799



Internal ID7034899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:81542908..81553016hg38UCSC Ensembl
Outerchr3:81592059..81602167hg19UCSC Ensembl
Outerchr3:81674749..81684857hg18UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg3810109
hg1910109
hg1810109
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1008470
Supporting Variants
SamplesHuRef
Known GenesGBE1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3563799
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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