A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893222



Internal ID18837356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:46142052..46231749hg38UCSC Ensembl
Outerchr19:46141945..46239987hg38UCSC Ensembl
Innerchr19:46645309..46735006hg19UCSC Ensembl
Outerchr19:46645202..46743244hg19UCSC Ensembl
Innerchr19:51337149..51426846hg18UCSC Ensembl
Outerchr19:51337042..51435084hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3898043
hg1998043
hg1898043
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787866, essv25788165
Samples
Known GenesDKFZp434J0226, IGFL1, IGFL2, RNU6-66P
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893222
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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