A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796579



Internal ID19181128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:57995793..58030314hg38UCSC Ensembl
Innerchr2:58222928..58257449hg19UCSC Ensembl
Innerchr2:58076432..58110953hg18UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3834522
hg1934522
hg1834522
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892537
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796579
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