A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866783



Internal ID22641718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:129898550..129941618hg38UCSC Ensembl
chr11:129768445..129811513hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3843069
hg1943069
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458573
Samples
Known GenesPRDM10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866783
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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