A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268391



Internal ID20835431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43196352..43197005hg38UCSC Ensembl
chr5:43196454..43197107hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38654
hg19654
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6561243
Supporting Variants
Samples
Known GenesNIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268391
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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