A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792162



Internal ID19162647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:135856124..135890512hg38UCSC Ensembl
Innerchr8:136868367..136902755hg19UCSC Ensembl
Innerchr8:136937549..136971937hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg3834389
hg1934389
hg1834389
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891487
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=14
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792162
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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