A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5495255



Internal ID272374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43318297..43318404hg38UCSC Ensembl
chr11:43339847..43339954hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17044017
Samples
Known GenesAPI5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5495255
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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