A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892745



Internal ID19183565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:100302409..100462916hg38UCSC Ensembl
Outerchr15:100226796..100468465hg38UCSC Ensembl
Innerchr15:100842614..101003121hg19UCSC Ensembl
Outerchr15:100767001..101008670hg19UCSC Ensembl
Innerchr15:98660137..98820644hg18UCSC Ensembl
Outerchr15:98584524..98826193hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38241670
hg19241670
hg18241670
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791027, essv25789683, essv25788257, essv25792601
Samples
Known GenesADAMTS17, CERS3, SPATA41
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892745
Frequency
Sample Size3017
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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