A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893340



Internal ID19184160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:44698618..44706933hg38UCSC Ensembl
Outerchr20:44698618..44706933hg38UCSC Ensembl
Innerchr20:43327259..43335574hg19UCSC Ensembl
Outerchr20:43327259..43335574hg19UCSC Ensembl
Innerchr20:42760673..42768988hg18UCSC Ensembl
Outerchr20:42760673..42768988hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg388316
hg198316
hg188316
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787314
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893340
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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