A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17623671



Internal ID21815718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6461282..6461282hg38UCSC Ensembl
chr19:6461293..6461293hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg382628
hg192628
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6105965
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17623671
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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