A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791027



Internal ID18829764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:100281371..100462916hg38UCSC Ensembl
Innerchr15:100821576..101003121hg19UCSC Ensembl
Innerchr15:98639099..98820644hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38181546
hg19181546
hg18181546
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892745
Supporting Variants
Samples
Known GenesADAMTS17, CERS3, SPATA41
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=47
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791027
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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