A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788165



Internal ID18825990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:46142052..46239987hg38UCSC Ensembl
Innerchr19:46645309..46743244hg19UCSC Ensembl
Innerchr19:51337149..51435084hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3897936
hg1997936
hg1897936
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893222
Supporting Variants
Samples
Known GenesDKFZp434J0226, IGFL1, IGFL2, RNU6-66P
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=30
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788165
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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