A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17980826



Internal ID20547866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46106523..46282986hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38176464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438829
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17980826
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0003


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