A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2422263



Internal ID7906360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167669616..168146724hg38UCSC Ensembl
Innerchr6:168070296..168547404hg19UCSC Ensembl
Innerchr6:167813145..168290253hg18UCSC Ensembl
Innerchr6:167888852..168365960hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38477109
hg19477109
hg18477109
hg17477109
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5161460
SamplesND04498
Known GenesC6orf123, FRMD1, HGC6.3, KIF25, KIF25-AS1, MLLT4, MLLT4-AS1
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)esv2422263
Frequency
Sample Size181
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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