A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5564079



Internal ID337001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10743612..10744379hg38UCSC Ensembl
chr16:10837469..10838236hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38768
hg19768
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17704527
Samples
Known GenesNUBP1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5564079
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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