A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17550168



Internal ID21874523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:968526..968526hg38UCSC Ensembl
chr5:968641..968641hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg382120
hg192120
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6060917
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17550168
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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