A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567204



Internal ID20940275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:80446001..80447053hg38UCSC Ensembl
chr5:79741820..79742872hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg381053
hg191053
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268979
Samples
Known GenesZFYVE16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567204
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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