A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17626180



Internal ID21818227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:54951129..54951129hg38UCSC Ensembl
chr16:54985041..54985041hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6080529
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17626180
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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