A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593047



Internal ID20966118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32993225..32994143hg38UCSC Ensembl
chr10:33282153..33283071hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38919
hg19919
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232263
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593047
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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