A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866486



Internal ID22641421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:113055640..113076035hg38UCSC Ensembl
chr11:112926362..112946757hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg3820396
hg1920396
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456722
Samples
Known GenesNCAM1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866486
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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