A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584459



Internal ID20957530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89604428..89605033hg38UCSC Ensembl
chr10:91364185..91364790hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38606
hg19606
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218786
Samples
Known GenesPANK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584459
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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