A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5584606



Internal ID21533148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:28430725..28430900hg38UCSC Ensembl
chr11:28452272..28452447hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17074143
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5584606
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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