A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17567971



Internal ID21760014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:159772729..159772729hg38UCSC Ensembl
chr5:159199736..159199736hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6071306
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17567971
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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