A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268769



Internal ID20835809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:155085433..155087646hg38UCSC Ensembl
chr5:154464993..154467206hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg382214
hg192214
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565521
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268769
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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