A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5161505



Internal ID8252839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167844897..168037992hg38UCSC Ensembl
Innerchr6:168245577..168438672hg19UCSC Ensembl
Innerchr6:167988426..168181521hg18UCSC Ensembl
Innerchr6:168064133..168257228hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38193096
hg19193096
hg18193096
hg17193096
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2422479
Supporting Variants
SamplesND03830
Known GenesHGC6.3, KIF25, KIF25-AS1, MLLT4
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)essv5161505
Frequency
Sample Size181
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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