A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561603



Internal ID334577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65884228..65884264hg38UCSC Ensembl
chr11:65651699..65651735hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg381240
hg191240
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17046795
Samples
Known GenesFIBP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561603
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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