A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560580



Internal ID20933651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:59596459..59598698hg38UCSC Ensembl
chr8:60509018..60511257hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg382240
hg192240
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278363
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560580
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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