A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796762



Internal ID18830875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:162002676..162027451hg38UCSC Ensembl
Innerchr5:161429682..161454457hg19UCSC Ensembl
Innerchr5:161362260..161387035hg18UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3824776
hg1924776
hg1824776
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890763
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796762
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