A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586227



Internal ID20959298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4080653..4083470hg38UCSC Ensembl
chr10:4122845..4125662hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg382818
hg192818
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234619
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586227
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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