A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796056



Internal ID19172695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:15093980..15148631hg38UCSC Ensembl
Innerchr17:14997297..15051948hg19UCSC Ensembl
Innerchr17:14938022..14992673hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3854652
hg1954652
hg1854652
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892963
Supporting Variants
Samples
Known GenesCDRT8
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=18
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796056
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