A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17634991



Internal ID21827038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8086039..8086039hg38UCSC Ensembl
chr19:8150923..8150923hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38345
hg19345
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6107181
Supporting Variants
Samples
Known GenesFBN3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17634991
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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