A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577324



Internal ID20950395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68351140..68352893hg38UCSC Ensembl
chr10:70110897..70112650hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381754
hg191754
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227763
Samples
Known GenesRUFY2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577324
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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