A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25781597



Internal ID18835318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:19192301..19227662hg38UCSC Ensembl
Innerchr8:19049811..19085172hg19UCSC Ensembl
Innerchr8:19094091..19129452hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3835362
hg1935362
hg1835362
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891368
Supporting Variants
Samples
Known GenesLOC100128993
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=24
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25781597
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