A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229277



Internal ID20796317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118699638..118700597hg38UCSC Ensembl
chr10:120459150..120460109hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38960
hg19960
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6589918
Supporting Variants
Samples
Known GenesCACUL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229277
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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