A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233872



Internal ID20800912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:49592375..49592844hg38UCSC Ensembl
chr14:50059093..50059562hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38470
hg19470
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6590857
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233872
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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