A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566182



Internal ID20939253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:23902512..23903765hg38UCSC Ensembl
chr8:23760025..23761278hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg381254
hg191254
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277518
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566182
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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