A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18270343



Internal ID20837383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:99237732..99262162hg38UCSC Ensembl
chr5:98573436..98597866hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg3824431
hg1924431
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559711
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18270343
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00015


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