A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17601198



Internal ID21793245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110839137..110839137hg38UCSC Ensembl
chr13:111491484..111491484hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6085807
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17601198
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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