A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5529382



Internal ID305403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11132002..11132229hg38UCSC Ensembl
chr16:11225859..11226086hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38228
hg19228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17704550
Samples
Known GenesCLEC16A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5529382
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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