A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098147



Internal ID21286982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:99729450..99874784hg38UCSC Ensembl
Innerchr15:100269655..100414989hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38145335
hg19145335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110817
Supporting Variants
Samplessample396
Known GenesDNM1P46, LYSMD4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098147
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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