A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892222



Internal ID19183042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:73630812..73687236hg38UCSC Ensembl
Outerchr12:73630812..73687236hg38UCSC Ensembl
Innerchr12:74024592..74081016hg19UCSC Ensembl
Outerchr12:74024592..74081016hg19UCSC Ensembl
Innerchr12:72310859..72367283hg18UCSC Ensembl
Outerchr12:72310859..72367283hg18UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg3856425
hg1956425
hg1856425
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782323
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892222
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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