A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18237163



Internal ID20804203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:60627411..60628036hg38UCSC Ensembl
chr14:61094129..61094754hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38626
hg19626
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588583
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18237163
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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