A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893239



Internal ID18837373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53100337..53123260hg38UCSC Ensembl
Outerchr19:53097592..53124524hg38UCSC Ensembl
Innerchr19:53603590..53626513hg19UCSC Ensembl
Outerchr19:53600845..53627777hg19UCSC Ensembl
Innerchr19:58295402..58318325hg18UCSC Ensembl
Outerchr19:58292657..58319589hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3826933
hg1926933
hg1826933
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798104, essv25786596, essv25789377, essv25789099, essv25787390
Samples
Known GenesZNF160, ZNF415
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893239
Frequency
Sample Size3017
Observed Gain2
Observed Loss3
Observed Complex0
Frequencyn/a


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