A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785585



Internal ID19163179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:60725485..61308324hg38UCSC Ensembl
Innerchr12:61119266..61702105hg19UCSC Ensembl
Innerchr12:59405533..59988372hg18UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg38582840
hg19582840
hg18582840
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892206
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=69
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785585
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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