A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893198



Internal ID19184018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:31980617..31993592hg38UCSC Ensembl
Outerchr19:31980617..31993592hg38UCSC Ensembl
Innerchr19:32471523..32484498hg19UCSC Ensembl
Outerchr19:32471523..32484498hg19UCSC Ensembl
Innerchr19:37163363..37176338hg18UCSC Ensembl
Outerchr19:37163363..37176338hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3812976
hg1912976
hg1812976
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799666
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893198
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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