A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786061



Internal ID19177145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:30108338..30152460hg38UCSC Ensembl
Innerchr12:30261271..30305393hg19UCSC Ensembl
Innerchr12:30152538..30196660hg18UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg3844123
hg1944123
hg1844123
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892171
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=14
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786061
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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