A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268386



Internal ID20835426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43141731..43142534hg38UCSC Ensembl
chr5:43141833..43142636hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38804
hg19804
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6562030
Supporting Variants
Samples
Known GenesZNF131
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268386
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00024


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