A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5511475



Internal ID288054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:38831939..38940355hg38UCSC Ensembl
chr11:38853489..38961905hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38108417
hg19108417
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17043759
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5511475
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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