A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559064



Internal ID20932135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:67082114..67083429hg38UCSC Ensembl
chr8:67994349..67995664hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg381316
hg191316
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278532
Samples
Known GenesCSPP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559064
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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