A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5161504



Internal ID8252688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160790139..161021345hg38UCSC Ensembl
Innerchr6:161211171..161442377hg19UCSC Ensembl
Innerchr6:161131161..161362367hg18UCSC Ensembl
Innerchr6:161181582..161412788hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38231207
hg19231207
hg18231207
hg17231207
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2422347
Supporting Variants
SamplesND01577
Known GenesMAP3K4
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)essv5161504
Frequency
Sample Size181
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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