A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797205



Internal ID19159595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:87179742..87232320hg38UCSC Ensembl
Innerchr8:88191970..88244548hg19UCSC Ensembl
Innerchr8:88261086..88313664hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3852579
hg1952579
hg1852579
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891433
Supporting Variants
Samples
Known GenesCNBD1
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797205
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