A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182065



Internal ID20749105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21419759..21460723hg38UCSC Ensembl
chr10:21708688..21749652hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3840965
hg1940965
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442703
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182065
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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