A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25781049



Internal ID19179991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:139008777..139029794hg38UCSC Ensembl
Innerchr8:140021020..140042037hg19UCSC Ensembl
Innerchr8:140090202..140111219hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3821018
hg1921018
hg1821018
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891491
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25781049
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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