A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113558



Internal ID21296824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:94843991..94846137hg38UCSC Ensembl
Innerchr15:95387220..95389366hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg382147
hg192147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14097180
Samplessample349
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113558
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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