A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238236



Internal ID20805277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:83513922..83514456hg38UCSC Ensembl
chr14:83980266..83980800hg19UCSC Ensembl
Cytoband14q31.2
Allele length
AssemblyAllele length
hg38535
hg19535
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588112
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238236
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0003


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