A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922752



Internal ID22697977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:21531009..21542731hg38UCSC Ensembl
chr11:21552555..21564277hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3811723
hg1911723
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17354056
Samples
Known GenesNELL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922752
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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