A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588244



Internal ID20961315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69128005..69128785hg38UCSC Ensembl
chr10:70887761..70888541hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38781
hg19781
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv798n223
Supporting Variantsnssv18217398
Samples
Known GenesVPS26A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588244
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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