A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560526



Internal ID333533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3529581..3532005hg38UCSC Ensembl
chr16:3579581..3582005hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg382425
hg192425
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17706370
Samples
Known GenesCLUAP1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560526
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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