A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594065



Internal ID20967136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63163953..63164854hg38UCSC Ensembl
chr10:64923713..64924614hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38902
hg19902
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218158
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594065
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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