A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236909



Internal ID20803949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:22571053..22571631hg38UCSC Ensembl
chr14:23039951..23040531hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38579
hg19581
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6590331
Supporting Variants
Samples
Known GenesDAD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236909
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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