A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268730



Internal ID20835770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:152288109..152582625hg38UCSC Ensembl
chr5:151667670..151962186hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg38294517
hg19294517
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6570431
Supporting Variants
Samples
Known GenesNMUR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268730
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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