A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17436686



Internal ID22494556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:104960294..105038066hg38UCSC Ensembl
chr8:105972522..106050294hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3877773
hg1977773
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5970816
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17436686
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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