A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18265101



Internal ID20832141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38092718..38093826hg38UCSC Ensembl
chr4:38094339..38095447hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg381109
hg191109
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568867
Supporting Variants
Samples
Known GenesTBC1D1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18265101
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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