A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915340



Internal ID22690558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60468084..60486983hg38UCSC Ensembl
chr11:60235557..60254456hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3818900
hg1918900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17367535
Samples
Known GenesMS4A1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915340
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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