A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225372



Internal ID20792412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:52129677..52130036hg38UCSC Ensembl
chr14:52596395..52596754hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38360
hg19360
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588763
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225372
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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