A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17608372



Internal ID21800419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:40443740..40448456hg38UCSC Ensembl
chr13:41017877..41022593hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg384717
hg194717
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6029812
Supporting Variants
Samples
Known GenesLINC00598
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17608372
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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