A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569210



Internal ID20942281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9506858..9507513hg38UCSC Ensembl
chr8:9364368..9365023hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38656
hg19656
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279155
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569210
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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