A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17604393



Internal ID21796440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:61331327..61334879hg38UCSC Ensembl
chr13:61905460..61909012hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg383553
hg193553
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6032560
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17604393
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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