A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5599977



Internal ID21548615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76567796..76567868hg38UCSC Ensembl
chr11:76278840..76278912hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17076164
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5599977
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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