A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6098039



Internal ID22007272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:51020032..51020032hg38UCSC Ensembl
chr16:51053943..51053943hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17626376
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6098039
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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