A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5514827



Internal ID291317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11429724..11506214hg38UCSC Ensembl
chr16:11523580..11600070hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3876491
hg1976491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17704573
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5514827
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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