A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569941



Internal ID20943012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:123405601..123405995hg38UCSC Ensembl
chr8:124417841..124418235hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38395
hg19395
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276123
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569941
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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