A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893250



Internal ID18837384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54906374..55000768hg38UCSC Ensembl
Outerchr19:54906374..55000768hg38UCSC Ensembl
Innerchr19:55417731..55512136hg19UCSC Ensembl
Outerchr19:55417731..55512136hg19UCSC Ensembl
Innerchr19:60109543..60203948hg18UCSC Ensembl
Outerchr19:60109543..60203948hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3894395
hg1994406
hg1894406
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796905
Samples
Known GenesNCR1, NLRP2, NLRP7, RNU6-35P, RNU6-64P
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893250
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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