A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18104740



Internal ID20671780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:96102141..96102447hg38UCSC Ensembl
chr3:95820985..95821291hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6364041
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18104740
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00055


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