A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268344



Internal ID20835384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:40770365..40770709hg38UCSC Ensembl
chr5:40770467..40770811hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg38345
hg19345
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6560285
Supporting Variants
Samples
Known GenesPRKAA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268344
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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