A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18237807



Internal ID20804847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:55109232..55109892hg38UCSC Ensembl
chr14:55575950..55576610hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg38661
hg19661
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579710
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18237807
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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