A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574799



Internal ID20947870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:100682426..100683307hg38UCSC Ensembl
chr8:101694654..101695535hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38882
hg19882
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275892
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574799
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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