A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5523356



Internal ID299598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3556218..3556311hg38UCSC Ensembl
chr16:3606219..3606312hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17706374
Samples
Known GenesNLRC3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5523356
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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