A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18275928



Internal ID20842968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102313273..102529231hg38UCSC Ensembl
chr8:103325501..103541459hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38215959
hg19215959
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565576
Supporting Variants
Samples
Known GenesUBR5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18275928
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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