A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278012



Internal ID20845052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:41455214..41456176hg38UCSC Ensembl
chr8:41312733..41313695hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38963
hg19963
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565480
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278012
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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