A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779900



Internal ID19179601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:60725485..61309626hg38UCSC Ensembl
Innerchr12:61119266..61703407hg19UCSC Ensembl
Innerchr12:59405533..59989674hg18UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg38584142
hg19584142
hg18584142
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=70
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779900
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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