A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278062



Internal ID20845102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42851486..42852568hg38UCSC Ensembl
chr8:42706629..42707711hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg381083
hg191083
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568495
Supporting Variants
Samples
Known GenesRNF170
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278062
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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