A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16264513



Internal ID20473731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7688892..7688956hg38UCSC Ensembl
chr19:7753778..7753842hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4742762
Supporting Variants
Samples
Known GenesFCER2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16264513
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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