A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17611966



Internal ID21804013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:47994838..48014758hg38UCSC Ensembl
chr14:48464041..48483961hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3819921
hg1919921
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6108167
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17611966
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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