A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866344



Internal ID22641279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:123307755..123310418hg38UCSC Ensembl
chr11:123178463..123181126hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg382664
hg192664
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461656
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866344
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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