A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560100



Internal ID20933171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:99662470..99662918hg38UCSC Ensembl
chr8:100674698..100675146hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg38449
hg19449
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279284
Samples
Known GenesVPS13B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560100
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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