A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18237142



Internal ID20804182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:59713714..59713777hg38UCSC Ensembl
chr14:60180432..60180495hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6577159
Supporting Variants
Samples
Known GenesRTN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18237142
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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