A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785959



Internal ID18827555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:48974027..49030531hg38UCSC Ensembl
Innerchr20:47590564..47647068hg19UCSC Ensembl
Innerchr20:47023971..47080475hg18UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3856505
hg1956505
hg1856505
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893345
Supporting Variants
Samples
Known GenesARFGEF2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785959
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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