A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17622077



Internal ID21814124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:131217..131217hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38262
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6082706
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17622077
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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