A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4762123



Internal ID20537983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66683139..66683139hg38UCSC Ensembl
chr16:66717042..66717042hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293449
Samples
Known GenesCMTM4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4762123
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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