A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17381906



Internal ID22439776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98568345..98590992hg38UCSC Ensembl
chr14:99034682..99057329hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3822648
hg1922648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5941197
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17381906
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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