A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16291400



Internal ID20500618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34543701..34559414hg38UCSC Ensembl
chr14:35012907..35028620hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3815714
hg1915714
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4761717
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16291400
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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