A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890930



Internal ID19185326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:115297469..115396178hg38UCSC Ensembl
Outerchr6:115297469..115396178hg38UCSC Ensembl
Innerchr6:115618633..115717342hg19UCSC Ensembl
Outerchr6:115618633..115717342hg19UCSC Ensembl
Innerchr6:115725326..115824035hg18UCSC Ensembl
Outerchr6:115725326..115824035hg18UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg3898710
hg1998710
hg1898710
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796906
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890930
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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