A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226192



Internal ID20793232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:9996494..9997004hg38UCSC Ensembl
chr10:10038457..10038967hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38511
hg19511
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6577889
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226192
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00026


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