A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268261



Internal ID20835301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:181254023..181254573hg38UCSC Ensembl
chr5:180681023..180681573hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38551
hg19551
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556522
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268261
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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