A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892155



Internal ID18839865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:18422620..18448504hg38UCSC Ensembl
Outerchr12:18405242..18470107hg38UCSC Ensembl
Innerchr12:18575554..18601438hg19UCSC Ensembl
Outerchr12:18558176..18623041hg19UCSC Ensembl
Innerchr12:18466821..18492705hg18UCSC Ensembl
Outerchr12:18449443..18514308hg18UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3864866
hg1964866
hg1864866
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787262, essv25779267
Samples
Known GenesPIK3C2G
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892155
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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