A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222994



Internal ID20790034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123543433..123544090hg38UCSC Ensembl
chr10:125302949..125303606hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38658
hg19658
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6577234
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222994
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00039


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