A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269603



Internal ID20836643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:30206142..30207498hg38UCSC Ensembl
chr5:30206249..30207605hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg381357
hg191357
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574016
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269603
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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