A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6087729



Internal ID21996962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58119788..58119788hg38UCSC Ensembl
chr16:58153692..58153692hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17628263
Samples
Known GenesC16orf80
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6087729
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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