A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892721



Internal ID18836855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:89530925..89673865hg38UCSC Ensembl
Outerchr15:89530925..89673865hg38UCSC Ensembl
Innerchr15:90074156..90217096hg19UCSC Ensembl
Outerchr15:90074156..90217096hg19UCSC Ensembl
Innerchr15:87875160..88018100hg18UCSC Ensembl
Outerchr15:87875160..88018100hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38142941
hg19142941
hg18142941
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791766, essv25791806
Samples
Known GenesKIF7, PLIN1, TICRR
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892721
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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