A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569889



Internal ID20942960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:97443359..97445974hg38UCSC Ensembl
chr8:98455587..98458202hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg382616
hg192616
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279186
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569889
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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