A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17602611



Internal ID21794658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:60202535..60202535hg38UCSC Ensembl
chr14:60669253..60669253hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38572
hg19572
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6089508
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17602611
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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