A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5515942



Internal ID292415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:56068757..56068850hg38UCSC Ensembl
chr16:56102669..56102762hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17706005
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5515942
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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