A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18237262



Internal ID20804302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74329122..74329783hg38UCSC Ensembl
chr14:74795825..74796486hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38662
hg19662
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6595030
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18237262
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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