A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891427



Internal ID19185823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:83337504..83422637hg38UCSC Ensembl
Outerchr8:83337504..83422637hg38UCSC Ensembl
Innerchr8:84249739..84334872hg19UCSC Ensembl
Outerchr8:84249739..84334872hg19UCSC Ensembl
Innerchr8:84412294..84497427hg18UCSC Ensembl
Outerchr8:84412294..84497427hg18UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3885134
hg1985134
hg1885134
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780397
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891427
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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