A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569603



Internal ID20942674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:12835786..12836823hg38UCSC Ensembl
chr8:12693295..12694332hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg381038
hg191038
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276231
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569603
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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