A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6077076



Internal ID21986309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:178258262..178258262hg38UCSC Ensembl
chr5:177685263..177685263hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17574528
Samples
Known GenesCOL23A1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6077076
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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