A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592335



Internal ID20965406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:83189771..83192475hg38UCSC Ensembl
chr10:84949527..84952231hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg382705
hg192705
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv829n223
Supporting Variantsnssv18224115
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592335
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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