A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892201



Internal ID19183021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:52288141..52305944hg38UCSC Ensembl
Outerchr12:52288141..52305944hg38UCSC Ensembl
Innerchr12:52681925..52699728hg19UCSC Ensembl
Outerchr12:52681925..52699728hg19UCSC Ensembl
Innerchr12:50968192..50985995hg18UCSC Ensembl
Outerchr12:50968192..50985995hg18UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg3817804
hg1917804
hg1817804
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797742
Samples
Known GenesKRT81, KRT86
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892201
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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