A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194733



Internal ID20761773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16275745..16302560hg38UCSC Ensembl
chr10:16317744..16344559hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3826816
hg1926816
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6454329
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194733
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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