A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25784792



Internal ID19178499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:6225032..6342924hg38UCSC Ensembl
Innerchr8:6082553..6200445hg19UCSC Ensembl
Innerchr8:6069961..6187853hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38117893
hg19117893
hg18117893
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891307
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=56
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25784792
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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