A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17625913



Internal ID21817960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16811666..16811666hg38UCSC Ensembl
chr19:16922477..16922477hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38415
hg19415
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6102087
Supporting Variants
Samples
Known GenesNWD1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17625913
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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