A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2422231



Internal ID7906328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:4100099..4233220hg38UCSC Ensembl
Innerchr6:4100333..4233454hg19UCSC Ensembl
Innerchr6:4045332..4178453hg18UCSC Ensembl
Innerchr6:4045332..4178453hg17UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38133122
hg19133122
hg18133122
hg17133122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5161552
SamplesND03627
Known GenesC6orf201, ECI2, LOC100507506
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)esv2422231
Frequency
Sample Size181
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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