A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594486



Internal ID20967557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92426124..92426644hg38UCSC Ensembl
chr10:94185881..94186401hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38521
hg19521
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223465
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594486
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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