A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787674



Internal ID19178042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:79804894..79815237hg38UCSC Ensembl
Innerchr5:79100717..79111060hg19UCSC Ensembl
Innerchr5:79136473..79146816hg18UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3810344
hg1910344
hg1810344
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890661
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 550
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787674
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