A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17555089



Internal ID21879444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:8467537..8467537hg38UCSC Ensembl
chr5:8467650..8467650hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6064720
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17555089
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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