A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893189



Internal ID19184009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:24421934..24446483hg38UCSC Ensembl
Outerchr19:24421934..24446483hg38UCSC Ensembl
Innerchr19:24604736..24629285hg19UCSC Ensembl
Outerchr19:24604736..24629285hg19UCSC Ensembl
Innerchr19:24396576..24421125hg18UCSC Ensembl
Outerchr19:24396576..24421125hg18UCSC Ensembl
Cytoband19p11
Allele length
AssemblyAllele length
hg3824550
hg1924550
hg1824550
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787110, essv25798579, essv25800631, essv25778397
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893189
Frequency
Sample Size3017
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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