A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890956



Internal ID19185352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:142026474..142055957hg38UCSC Ensembl
Outerchr6:142025608..142063866hg38UCSC Ensembl
Innerchr6:142347611..142377094hg19UCSC Ensembl
Outerchr6:142346745..142385003hg19UCSC Ensembl
Innerchr6:142389304..142418787hg18UCSC Ensembl
Outerchr6:142388438..142426696hg18UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3838259
hg1938259
hg1838259
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798036, essv25781385
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890956
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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