A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797911



Internal ID19166921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:115756017..115784737hg38UCSC Ensembl
Innerchr5:115091714..115120434hg19UCSC Ensembl
Innerchr5:115119613..115148333hg18UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3828721
hg1928721
hg1828721
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890717
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797911
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