A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558638



Internal ID20931709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:21291976..21292807hg38UCSC Ensembl
chr8:21149487..21150318hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38832
hg19832
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277452
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558638
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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