A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18237258



Internal ID20804298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74185375..74186143hg38UCSC Ensembl
chr14:74652078..74652846hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38769
hg19769
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6590921
Supporting Variants
Samples
Known GenesLIN52
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18237258
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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