A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266829



Internal ID20833869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138550067..138550642hg38UCSC Ensembl
chr5:137885756..137886331hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg38576
hg19576
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575409
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266829
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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