A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3948085



Internal ID21368154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86278758..86278758hg38UCSC Ensembl
chr16:86312364..86312364hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38186
hg19186
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15184889
SamplesHG002
Known GenesLINC01081
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3948085
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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