A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25784709



Internal ID19168528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:6682887..6699111hg38UCSC Ensembl
Innerchr5:6683000..6699224hg19UCSC Ensembl
Innerchr5:6736000..6752224hg18UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3816225
hg1916225
hg1816225
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894118
Supporting Variants
Samples
Known GenesLOC100505625
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25784709
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