A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17363807



Internal ID22589476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60044497..60225612hg38UCSC Ensembl
chr11:59811970..59993085hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38181116
hg19181116
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5908038
Supporting Variants
Samples
Known GenesMS4A2, MS4A3, MS4A6A, OOSP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17363807
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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