A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893286



Internal ID19184106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:10067958..10077600hg38UCSC Ensembl
Outerchr20:10067958..10077600hg38UCSC Ensembl
Innerchr20:10048606..10058248hg19UCSC Ensembl
Outerchr20:10048606..10058248hg19UCSC Ensembl
Innerchr20:9996606..10006248hg18UCSC Ensembl
Outerchr20:9996606..10006248hg18UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg389643
hg199643
hg189643
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787487
Samples
Known GenesSNAP25-AS1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893286
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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