A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892263



Internal ID18836397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:104485495..104492606hg38UCSC Ensembl
Outerchr12:104485495..104492606hg38UCSC Ensembl
Innerchr12:104879273..104886384hg19UCSC Ensembl
Outerchr12:104879273..104886384hg19UCSC Ensembl
Innerchr12:103403403..103410514hg18UCSC Ensembl
Outerchr12:103403403..103410514hg18UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg387112
hg197112
hg187112
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783170
Samples
Known GenesCHST11
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892263
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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