A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238669



Internal ID20805709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73436579..73436808hg38UCSC Ensembl
chr14:73903287..73903516hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38230
hg19230
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581569
Supporting Variants
Samples
Known GenesNUMB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238669
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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