A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18099181



Internal ID20666221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4091342..4102611hg38UCSC Ensembl
chr3:4133026..4144295hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3811270
hg1911270
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6367331
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18099181
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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