A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223074



Internal ID20790114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125854909..125855429hg38UCSC Ensembl
chr10:127543478..127543998hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg38521
hg19521
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6583789
Supporting Variants
Samples
Known GenesDHX32
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223074
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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