A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892419



Internal ID18836553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:88893389..89807811hg38UCSC Ensembl
Outerchr13:88893389..89807811hg38UCSC Ensembl
Innerchr13:89545643..90460065hg19UCSC Ensembl
Outerchr13:89545643..90460065hg19UCSC Ensembl
Innerchr13:88343644..89258066hg18UCSC Ensembl
Outerchr13:88343644..89258066hg18UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg38914423
hg19914423
hg18914423
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25793007
Samples
Known GenesLINC00353
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892419
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer