A curated catalogue of human genomic structural variation




Variant Details

Variant: esv989863



Internal ID7076448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:106675927..106677022hg38UCSC Ensembl
Outerchr6:107123802..107124897hg19UCSC Ensembl
Outerchr6:107230495..107231590hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381096
hg191096
hg181096
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565140
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv989863
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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