A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17626086



Internal ID21818133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:47181433..47181490hg38UCSC Ensembl
chr16:47215344..47215401hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6020649
Supporting Variants
Samples
Known GenesITFG1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17626086
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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