A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860132



Internal ID22635067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:99424779..99425878hg38UCSC Ensembl
chr11:99295510..99296609hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17451713
Samples
Known GenesCNTN5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860132
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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