A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115126



Internal ID21298392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:14836104..14898443hg38UCSC Ensembl
Innerchr17:14739421..14801760hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3862340
hg1962340
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14098083
Samplessample66
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115126
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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