A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17603856



Internal ID21795903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:73016998..73021778hg38UCSC Ensembl
chr13:73591136..73595916hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg384781
hg194781
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6031651
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17603856
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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