A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18092858



Internal ID20659898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:115279993..115280406hg38UCSC Ensembl
chr3:114998840..114999253hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg38414
hg19414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6372495
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18092858
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00064


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