A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5596141



Internal ID21544748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:83899032..83899294hg38UCSC Ensembl
chr11:83610075..83610337hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38263
hg19263
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17076282
SamplesHG02818
Known GenesDLG2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5596141
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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