A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18092850



Internal ID20659890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:115219130..115220727hg38UCSC Ensembl
chr3:114937977..114939574hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg381598
hg191598
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6365255
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18092850
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00033


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