A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18237638



Internal ID20804678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:90031032..90031391hg38UCSC Ensembl
chr14:90497376..90497735hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38360
hg19360
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587376
Supporting Variants
Samples
Known GenesTDP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18237638
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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