A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893197



Internal ID19184017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:28187430..28238686hg38UCSC Ensembl
Outerchr19:28187430..28238686hg38UCSC Ensembl
Innerchr19:28678337..28729593hg19UCSC Ensembl
Outerchr19:28678337..28729593hg19UCSC Ensembl
Innerchr19:33370177..33421433hg18UCSC Ensembl
Outerchr19:33370177..33421433hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3851257
hg1951257
hg1851257
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779739
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893197
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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