A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893257



Internal ID19184077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:57309349..57333965hg38UCSC Ensembl
Outerchr19:57309349..57333965hg38UCSC Ensembl
Innerchr19:57820717..57845333hg19UCSC Ensembl
Outerchr19:57820717..57845333hg19UCSC Ensembl
Innerchr19:62512529..62537145hg18UCSC Ensembl
Outerchr19:62512529..62537145hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3824617
hg1924617
hg1824617
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797346, essv25797323
Samples
Known GenesZNF543
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893257
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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