A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267087



Internal ID20834127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:74655766..74656556hg38UCSC Ensembl
chr5:73951591..73952381hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38791
hg19791
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6569723
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267087
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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