A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779197



Internal ID19161354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:110111157..110300884hg38UCSC Ensembl
Innerchr5:109446858..109636585hg19UCSC Ensembl
Innerchr5:109474757..109664484hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38189728
hg19189728
hg18189728
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890708
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=39
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779197
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