A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18099197



Internal ID20666237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:41048350..41103598hg38UCSC Ensembl
chr3:41089841..41145089hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3855249
hg1955249
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6364192
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18099197
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00041


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