A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17542667



Internal ID21867022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2099237..2099237hg38UCSC Ensembl
chr5:2099351..2099351hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38355
hg19355
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6061178
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17542667
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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