A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6094339



Internal ID22003572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:137921..137921hg38UCSC Ensembl
chr16:187920..187920hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17613671
Samples
Known GenesNPRL3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6094339
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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