A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5509275



Internal ID285936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:129236310..129240260hg38UCSC Ensembl
chr11:129106205..129110155hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg383951
hg193951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17052641
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5509275
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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