A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579828



Internal ID20952899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101904743..101907386hg38UCSC Ensembl
chr10:103664500..103667143hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg382644
hg192644
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230061
Samples
Known GenesC10orf76
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579828
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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