A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228942



Internal ID20795982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59627364..59628026hg38UCSC Ensembl
chr10:61387122..61387784hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38663
hg19663
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6577868
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228942
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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