A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17612930



Internal ID21804977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:35213376..35213376hg38UCSC Ensembl
chr13:35787513..35787513hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38296
hg19296
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6087386
Supporting Variants
Samples
Known GenesNBEA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17612930
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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