A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17615069



Internal ID21807116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2811453..2811453hg38UCSC Ensembl
chr16:2861454..2861454hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6092508
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17615069
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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