A curated catalogue of human genomic structural variation




Variant Details

Variant: essv84207



Internal ID11303518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31391871..31489801hg38UCSC Ensembl
Innerchr6:31359648..31457578hg19UCSC Ensembl
Innerchr6:31467627..31565557hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3897931
hg1997931
hg1897931
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv29968
Supporting Variants
SamplesHuRef
Known GenesHCG26, HCP5, MICA
MethodMerging
AnalysisNo Reference, merging experiment
PlatformNot Reported
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv84207
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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