A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892171



Internal ID19186567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:30108338..30152460hg38UCSC Ensembl
Outerchr12:30108338..30152460hg38UCSC Ensembl
Innerchr12:30261271..30305393hg19UCSC Ensembl
Outerchr12:30261271..30305393hg19UCSC Ensembl
Innerchr12:30152538..30196660hg18UCSC Ensembl
Outerchr12:30152538..30196660hg18UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg3844123
hg1944123
hg1844123
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786061
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892171
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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