A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5596392



Internal ID21545000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:129744407..129744540hg38UCSC Ensembl
chr11:129614302..129614435hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17073502
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5596392
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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