A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567105



Internal ID20940176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:26107826..26108277hg38UCSC Ensembl
chr8:25965342..25965793hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38452
hg19452
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277561
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567105
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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