A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595351



Internal ID20968422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:85018158..85036191hg38UCSC Ensembl
chr10:86777914..86795947hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3818034
hg1918034
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232746
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595351
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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