A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17598168



Internal ID21790212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:59220084..59220084hg38UCSC Ensembl
chr13:59794218..59794218hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6099773
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17598168
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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