A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5495844



Internal ID272940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59528621..59528694hg38UCSC Ensembl
chr11:59296094..59296167hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17045515
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5495844
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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