A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5511469



Internal ID288048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:29379511..29401227hg38UCSC Ensembl
chr11:29401058..29422774hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3821717
hg1921717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17043050
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5511469
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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