A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797742



Internal ID19165970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:52288141..52305944hg38UCSC Ensembl
Innerchr12:52681925..52699728hg19UCSC Ensembl
Innerchr12:50968192..50985995hg18UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg3817804
hg1917804
hg1817804
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892201
Supporting Variants
Samples
Known GenesKRT81, KRT86
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797742
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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