A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17735824



Internal ID159490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:73124231..73146430hg38UCSC Ensembl
chr8:74036466..74058665hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3822200
hg1922200
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556691
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17735824
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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