A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979655



Internal ID20546695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:22121001..22124600hg38UCSC Ensembl
chr10:22409930..22413529hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg383600
hg193600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6443420
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979655
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.01058


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