A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17606449



Internal ID21798496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:49590364..49590419hg38UCSC Ensembl
chr14:50057082..50057137hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6028687
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17606449
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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