A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5585291



Internal ID21533837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33665869..33665927hg38UCSC Ensembl
chr11:33687415..33687473hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17074568
SamplesNA18534
Known GenesKIAA1549L
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5585291
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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