A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893182



Internal ID18837316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:22163601..23022762hg38UCSC Ensembl
Outerchr19:22155340..23022762hg38UCSC Ensembl
Innerchr19:22346403..23205564hg19UCSC Ensembl
Outerchr19:22338142..23205564hg19UCSC Ensembl
Innerchr19:22138243..22997404hg18UCSC Ensembl
Outerchr19:22129982..22997404hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38867423
hg19867423
hg18867423
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791646, essv25788864, essv25792590
Samples
Known GenesLOC100996349, LOC440518, ZNF492, ZNF676, ZNF728, ZNF729, ZNF98, ZNF99
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893182
Frequency
Sample Size3017
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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