A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567533



Internal ID20940604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:117831178..117831736hg38UCSC Ensembl
chr5:117166873..117167431hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38559
hg19559
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5909n223
Supporting Variantsnssv18266641
Samples
Known GenesLOC102467224
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567533
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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