A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5501347



Internal ID278246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65956123..65960630hg38UCSC Ensembl
chr11:65723594..65728101hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg384508
hg194508
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17046800
Samples
Known GenesTSGA10IP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5501347
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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