A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5601770



Internal ID21550420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1554280..1554389hg38UCSC Ensembl
chr11:1575510..1575619hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17073738
SamplesHG02818
Known GenesDUSP8, MOB2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5601770
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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