A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893220



Internal ID18837354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43658802..43706225hg38UCSC Ensembl
Outerchr19:43658802..43706225hg38UCSC Ensembl
Innerchr19:44162954..44210377hg19UCSC Ensembl
Outerchr19:44162954..44210377hg19UCSC Ensembl
Innerchr19:48854794..48902217hg18UCSC Ensembl
Outerchr19:48854794..48902217hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3847424
hg1947424
hg1847424
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788662
Samples
Known GenesPLAUR
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893220
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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