A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278530



Internal ID20845570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:67069877..67070365hg38UCSC Ensembl
chr8:67982112..67982600hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg38489
hg19489
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6566702
Supporting Variants
Samples
Known GenesCSPP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278530
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00035


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