A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855301



Internal ID22630236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63313988..63316021hg38UCSC Ensembl
chr11:63081460..63083493hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg382034
hg192034
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465422
Samples
Known GenesMIR3680-1, MIR3680-2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855301
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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