A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892156



Internal ID19186552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:18938243..19028300hg38UCSC Ensembl
Outerchr12:18938243..19028300hg38UCSC Ensembl
Innerchr12:19091177..19181234hg19UCSC Ensembl
Outerchr12:19091177..19181234hg19UCSC Ensembl
Innerchr12:18982444..19072501hg18UCSC Ensembl
Outerchr12:18982444..19072501hg18UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3890058
hg1990058
hg1890058
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788379
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892156
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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