A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17620324



Internal ID21812371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:60770396..60770396hg38UCSC Ensembl
chr16:60804300..60804300hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6097029
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17620324
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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