A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583036



Internal ID20956107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89721658..89721931hg38UCSC Ensembl
chr10:91481415..91481688hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38274
hg19274
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223828
Samples
Known GenesKIF20B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583036
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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