A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5589991



Internal ID21538559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96399541..96400072hg38UCSC Ensembl
chr11:96132705..96133236hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38532
hg19532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17076458
SamplesHG01114
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5589991
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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