A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892186



Internal ID19183006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:37678971..38179560hg38UCSC Ensembl
Outerchr12:37571120..38194590hg38UCSC Ensembl
Innerchr12:38072773..38573362hg19UCSC Ensembl
Outerchr12:37964922..38588392hg19UCSC Ensembl
Innerchr12:36359040..36859629hg18UCSC Ensembl
Outerchr12:36251189..36874659hg18UCSC Ensembl
Cytoband12q11
Allele length
AssemblyAllele length
hg38623471
hg19623471
hg18623471
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789886, essv25788155
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892186
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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