A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893067



Internal ID19183887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:5834954..5843070hg38UCSC Ensembl
Outerchr18:5832774..5843070hg38UCSC Ensembl
Innerchr18:5834953..5843069hg19UCSC Ensembl
Outerchr18:5832773..5843069hg19UCSC Ensembl
Innerchr18:5824953..5833069hg18UCSC Ensembl
Outerchr18:5822773..5833069hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3810297
hg1910297
hg1810297
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796320, essv25796466, essv25783107
Samples
Known GenesMIR3976
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893067
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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