A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5590091



Internal ID21538659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:75878262..75878341hg38UCSC Ensembl
chr11:75589306..75589385hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17075897
SamplesHG03486
Known GenesUVRAG
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5590091
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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