A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17606253



Internal ID21798300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109488970..109489257hg38UCSC Ensembl
chr13:110141317..110141604hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38288
hg19288
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6025923
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17606253
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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