A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779267



Internal ID18825759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:18405242..18448504hg38UCSC Ensembl
Innerchr12:18558176..18601438hg19UCSC Ensembl
Innerchr12:18449443..18492705hg18UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3843263
hg1943263
hg1843263
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892155
Supporting Variants
Samples
Known GenesPIK3C2G
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=14
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779267
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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