A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17607240



Internal ID21799287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:79383040..79383040hg38UCSC Ensembl
chr13:79957175..79957175hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6089128
Supporting Variants
Samples
Known GenesRBM26
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17607240
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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