A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16284128



Internal ID20493346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:50487670..50487740hg38UCSC Ensembl
chr19:50990927..50990997hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4748746
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16284128
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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