A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5161278



Internal ID8252724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:66139360..66206913hg38UCSC Ensembl
Innerchr6:66849253..66916806hg19UCSC Ensembl
Innerchr6:66905974..66973527hg18UCSC Ensembl
Innerchr6:66905974..66973527hg17UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3867554
hg1967554
hg1867554
hg1767554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2422329
Supporting Variants
SamplesND01684
Known Genes
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)essv5161278
Frequency
Sample Size181
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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