A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892163



Internal ID18839873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:25052307..25059107hg38UCSC Ensembl
Outerchr12:25052307..25059107hg38UCSC Ensembl
Innerchr12:25205241..25212041hg19UCSC Ensembl
Outerchr12:25205241..25212041hg19UCSC Ensembl
Innerchr12:25096508..25103308hg18UCSC Ensembl
Outerchr12:25096508..25103308hg18UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg386801
hg196801
hg186801
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797128
Samples
Known GenesLRMP
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892163
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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