A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224631



Internal ID20791671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:49938702..49939052hg38UCSC Ensembl
chr14:50405420..50405770hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38351
hg19351
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6593651
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224631
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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