A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568507



Internal ID20941578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:43023015..43023771hg38UCSC Ensembl
chr8:42878158..42878914hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38757
hg19757
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278085
Samples
Known GenesHOOK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568507
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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