A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559844



Internal ID20932915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94840914..94842086hg38UCSC Ensembl
chr8:95853142..95854314hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg381173
hg191173
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279133
Samples
Known GenesINTS8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559844
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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