A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5495821



Internal ID272917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118410532..118410588hg38UCSC Ensembl
chr11:118281247..118281303hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17053602
Samples
Known GenesLOC100131626
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5495821
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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