A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16264018



Internal ID20473236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:5569877..5570046hg38UCSC Ensembl
chr19:5569888..5570057hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4736237
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16264018
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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