A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969983



Internal ID22744918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43335390..43335390hg38UCSC Ensembl
chr11:43356940..43356940hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17362428
Samples
Known GenesAPI5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969983
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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