A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785399



Internal ID19174536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:7184078..7377776hg38UCSC Ensembl
Innerchr20:7164725..7358423hg19UCSC Ensembl
Innerchr20:7112725..7306423hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38193699
hg19193699
hg18193699
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893278
Supporting Variants
Samples
Known GenesMIR8062
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=41
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785399
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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