A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25801053



Internal ID19181591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:77639466..77721032hg38UCSC Ensembl
Innerchr8:78551702..78633267hg19UCSC Ensembl
Innerchr8:78714257..78795822hg18UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg3881567
hg1981566
hg1881566
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891418
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=14
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25801053
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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