A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25784706



Internal ID19177813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:69066747..69110716hg38UCSC Ensembl
Innerchr13:69640879..69684848hg19UCSC Ensembl
Innerchr13:68538880..68582849hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3843970
hg1943970
hg1843970
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892384
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=13
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25784706
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