A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893255



Internal ID19184075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:56898287..56925028hg38UCSC Ensembl
Outerchr19:56898287..56925028hg38UCSC Ensembl
Innerchr19:57409655..57436396hg19UCSC Ensembl
Outerchr19:57409655..57436396hg19UCSC Ensembl
Innerchr19:62101467..62128208hg18UCSC Ensembl
Outerchr19:62101467..62128208hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3826742
hg1926742
hg1826742
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787736
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 550
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893255
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer