A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559898



Internal ID20932969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:128891466..128891661hg38UCSC Ensembl
chr8:129903712..129903907hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276237
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559898
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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