A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890867



Internal ID19185169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:65412466..65436926hg38UCSC Ensembl
Outerchr6:65412466..65436926hg38UCSC Ensembl
Innerchr6:66122359..66146819hg19UCSC Ensembl
Outerchr6:66122359..66146819hg19UCSC Ensembl
Innerchr6:66179080..66203540hg18UCSC Ensembl
Outerchr6:66179080..66203540hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3824461
hg1924461
hg1824461
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25778641
Samples
Known GenesEYS
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890867
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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