A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268104



Internal ID20835144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:165026339..165027798hg38UCSC Ensembl
chr5:164453345..164454804hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg381460
hg191460
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6562127
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268104
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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