A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17623723



Internal ID21815770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:63215807..63215807hg38UCSC Ensembl
chr16:63249711..63249711hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6091766
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17623723
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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