A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565298



Internal ID7036680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:105594253..105605644hg38UCSC Ensembl
Outerchr6:106042128..106053519hg19UCSC Ensembl
Outerchr6:106148821..106160212hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3811392
hg1911392
hg1811392
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1006531
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565298
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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