A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573361



Internal ID20946432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:104511092..104512208hg38UCSC Ensembl
chr8:105523320..105524436hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg381117
hg191117
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276324
Samples
Known GenesLRP12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573361
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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