A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17619260



Internal ID21811307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12803154..12803154hg38UCSC Ensembl
chr19:12913968..12913968hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg382454
hg192454
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6100804
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17619260
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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