A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892139



Internal ID19186535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:10522696..10545656hg38UCSC Ensembl
Outerchr12:10522696..10545656hg38UCSC Ensembl
Innerchr12:10675295..10698255hg19UCSC Ensembl
Outerchr12:10675295..10698255hg19UCSC Ensembl
Innerchr12:10566562..10589522hg18UCSC Ensembl
Outerchr12:10566562..10589522hg18UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3822961
hg1922961
hg1822961
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798320
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892139
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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