A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25801487



Internal ID19170168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:109249649..109265014hg38UCSC Ensembl
Innerchr13:109901997..109917362hg19UCSC Ensembl
Innerchr13:108699998..108715363hg18UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3815366
hg1915366
hg1815366
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892446
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25801487
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