A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5503886



Internal ID280698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:13906856..13907738hg38UCSC Ensembl
chr11:13928403..13929285hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38883
hg19883
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17041374
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5503886
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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