A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17608091



Internal ID21800138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:49643021..49643214hg38UCSC Ensembl
chr14:50109739..50109932hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38194
hg19194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6032615
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17608091
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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