A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797323



Internal ID19177006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:57309349..57333965hg38UCSC Ensembl
Innerchr19:57820717..57845333hg19UCSC Ensembl
Innerchr19:62512529..62537145hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3824617
hg1924617
hg1824617
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893257
Supporting Variants
Samples
Known GenesZNF543
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797323
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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