A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791806



Internal ID18813343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:89530925..89673865hg38UCSC Ensembl
Innerchr15:90074156..90217096hg19UCSC Ensembl
Innerchr15:87875160..88018100hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38142941
hg19142941
hg18142941
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892721
Supporting Variants
Samples
Known GenesKIF7, PLIN1, TICRR
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=24
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791806
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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