A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6098826



Internal ID22008059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4211456..4211456hg38UCSC Ensembl
chr16:4261457..4261457hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607270
Samples
Known GenesSRL
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6098826
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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