A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586757



Internal ID20959828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102540451..102541698hg38UCSC Ensembl
chr10:104300208..104301455hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg381248
hg191248
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217412
Samples
Known GenesSUFU
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586757
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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