A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238227



Internal ID20805268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:82746865..82747394hg38UCSC Ensembl
chr14:83213209..83213738hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg38530
hg19530
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579054
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238227
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00035


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