A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562282



Internal ID20935353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101183222..101183974hg38UCSC Ensembl
chr8:102195450..102196202hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38753
hg19753
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7440n223
Supporting Variantsnssv18275911
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562282
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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