A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16945513



Internal ID31007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:10667741..10667847hg38UCSC Ensembl
chr4:10669365..10669471hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5440314
Supporting Variants
Samples
Known GenesCLNK
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16945513
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.37699


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