A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17623489



Internal ID21815536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81704622..81704622hg38UCSC Ensembl
chr16:81738227..81738227hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38369
hg19369
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6097185
Supporting Variants
Samples
Known GenesCMIP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17623489
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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