A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17599660



Internal ID21791706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:49920823..49920879hg38UCSC Ensembl
chr14:50387541..50387597hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6026217
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17599660
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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