A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890919



Internal ID19185315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:102272041..102304525hg38UCSC Ensembl
Outerchr6:102272041..102304525hg38UCSC Ensembl
Innerchr6:102719916..102752400hg19UCSC Ensembl
Outerchr6:102719916..102752400hg19UCSC Ensembl
Innerchr6:102826609..102859093hg18UCSC Ensembl
Outerchr6:102826609..102859093hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3832485
hg1932485
hg1832485
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785860
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890919
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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