A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5498615



Internal ID275605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:133900029..133900387hg38UCSC Ensembl
chr11:133769924..133770282hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38359
hg19359
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17051751
Samples
Known GenesMIR4697HG
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5498615
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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