A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17627066



Internal ID21819113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12693707..12694149hg38UCSC Ensembl
chr19:12804521..12804963hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38443
hg19443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6056024
Supporting Variants
Samples
Known GenesFBXW9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17627066
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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