A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25781194



Internal ID19168903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:7824755..7905327hg38UCSC Ensembl
Innerchr12:7977351..8057923hg19UCSC Ensembl
Innerchr12:7868618..7949190hg18UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3880573
hg1980573
hg1880573
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892130
Supporting Variants
Samples
Known GenesSLC2A14
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=32
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25781194
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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