A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799328



Internal ID19166707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:57153231..57190904hg38UCSC Ensembl
Innerchr8:58065790..58103463hg19UCSC Ensembl
Innerchr8:58228344..58266017hg18UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3837674
hg1937674
hg1837674
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891399
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799328
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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