A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563093



Internal ID20936164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:104332593..104333153hg38UCSC Ensembl
chr8:105344821..105345381hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38561
hg19561
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276321
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563093
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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