A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560372



Internal ID333380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67329498..67343502hg38UCSC Ensembl
chr16:67363401..67377405hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3814005
hg1914005
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17707495
Samples
Known GenesLRRC36
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560372
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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