A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115091



Internal ID21298357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:17527255..17537349hg38UCSC Ensembl
Innerchr1:17853751..17863844hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3810095
hg1910094
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8n145
Supporting Variantsnssv14095267
Samplessample339
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115091
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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