A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5161473



Internal ID7906187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:4100099..4377162hg38UCSC Ensembl
Innerchr6:4100333..4377396hg19UCSC Ensembl
Innerchr6:4045332..4322395hg18UCSC Ensembl
Innerchr6:4045332..4322395hg17UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38277064
hg19277064
hg18277064
hg17277064
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2422457
Supporting Variants
SamplesND04845
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)essv5161473
Frequency
Sample Size181
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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