A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16290398



Internal ID20499616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60460682..60461903hg38UCSC Ensembl
chr11:60228155..60229376hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg381222
hg191222
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4750140
Supporting Variants
Samples
Known GenesMS4A1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16290398
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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