A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5495889



Internal ID272984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:11814539..11821322hg38UCSC Ensembl
chr11:11836086..11842869hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg386784
hg196784
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17042850
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5495889
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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