A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17387206



Internal ID22445076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98972786..98973472hg38UCSC Ensembl
chr14:99439123..99439809hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38687
hg19687
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5938850
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17387206
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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