A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16276754



Internal ID20485972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8051185..8051273hg38UCSC Ensembl
chr19:8116069..8116157hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730836
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16276754
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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