A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6144896



Internal ID344101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:26402486..26408743hg38UCSC Ensembl
chr16:26413807..26420064hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg386258
hg196258
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17706221
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6144896
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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