A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853932



Internal ID22628867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108209997..108217118hg38UCSC Ensembl
chr11:108080724..108087845hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg387122
hg197122
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17466159
Samples
Known GenesNPAT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853932
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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