A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559688



Internal ID20932759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:20833862..20835365hg38UCSC Ensembl
chr8:20691373..20692876hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg381504
hg191504
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277447
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559688
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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