A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565042



Internal ID20938113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:83487722..83489032hg38UCSC Ensembl
chr8:84399957..84401267hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg381311
hg191311
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278872
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565042
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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