A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5591200



Internal ID21539773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65970794..65970912hg38UCSC Ensembl
chr11:65738265..65738383hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17075418
SamplesHG03125
Known GenesSART1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5591200
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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