A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269417



Internal ID20836457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:157163790..157164323hg38UCSC Ensembl
chr5:156590801..156591334hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38534
hg19534
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6563381
Supporting Variants
Samples
Known GenesFAM71B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269417
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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