A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17629157



Internal ID21821204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:56397719..56397719hg38UCSC Ensembl
chr16:56431631..56431631hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6098650
Supporting Variants
Samples
Known GenesAMFR
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17629157
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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