A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591847



Internal ID20964918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68880000..68880121hg38UCSC Ensembl
chr10:70639756..70639877hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223354
Samples
Known GenesSTOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591847
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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