A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17523770



Internal ID21848129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:121766870..121766870hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38471
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6058776
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17523770
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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