A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591462



Internal ID20964533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112407306..112408121hg38UCSC Ensembl
chr10:114167064..114167879hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38816
hg19816
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220612
Samples
Known GenesACSL5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591462
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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