A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892162



Internal ID19186558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:24631205..24695167hg38UCSC Ensembl
Outerchr12:24631205..24695167hg38UCSC Ensembl
Innerchr12:24784139..24848101hg19UCSC Ensembl
Outerchr12:24784139..24848101hg19UCSC Ensembl
Innerchr12:24675406..24739368hg18UCSC Ensembl
Outerchr12:24675406..24739368hg18UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg3863963
hg1963963
hg1863963
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786318
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892162
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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