A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859044



Internal ID22633979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:129803551..129807051hg38UCSC Ensembl
chr11:129673446..129676946hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg383501
hg193501
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465069
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859044
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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