A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17630563



Internal ID21822610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:51755558..51755558hg38UCSC Ensembl
chr16:51789469..51789469hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6080954
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17630563
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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