A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5592167



Internal ID21540748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32522014..32522065hg38UCSC Ensembl
chr11:32543560..32543611hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17074000
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5592167
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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