A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780397



Internal ID19163839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:83337504..83422637hg38UCSC Ensembl
Innerchr8:84249739..84334872hg19UCSC Ensembl
Innerchr8:84412294..84497427hg18UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3885134
hg1985134
hg1885134
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891427
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=15
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780397
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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