A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17613417



Internal ID21805464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:43879802..43879802hg38UCSC Ensembl
chr13:44453938..44453938hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6092837
Supporting Variants
Samples
Known GenesLACC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17613417
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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