A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893260



Internal ID18837394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:58088681..58218467hg38UCSC Ensembl
Outerchr19:58088681..58218467hg38UCSC Ensembl
Innerchr19:58600048..58729833hg19UCSC Ensembl
Outerchr19:58600048..58729833hg19UCSC Ensembl
Innerchr19:63291860..63421645hg18UCSC Ensembl
Outerchr19:63291860..63421645hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38129787
hg19129786
hg18129786
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789754
Samples
Known GenesZNF274, ZNF329, ZSCAN18
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893260
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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