A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892144



Internal ID19186540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:12864177..12873120hg38UCSC Ensembl
Outerchr12:12864177..12873120hg38UCSC Ensembl
Innerchr12:13017111..13026054hg19UCSC Ensembl
Outerchr12:13017111..13026054hg19UCSC Ensembl
Innerchr12:12908378..12917321hg18UCSC Ensembl
Outerchr12:12908378..12917321hg18UCSC Ensembl
Cytoband12p13.1
Allele length
AssemblyAllele length
hg388944
hg198944
hg188944
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799498
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892144
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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