A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266559



Internal ID20833599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:67686820..67687262hg38UCSC Ensembl
chr4:68552538..68552980hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38443
hg19443
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556598
Supporting Variants
Samples
Known GenesUBA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266559
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00023


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