A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17592260



Internal ID21784303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60704844..60704897hg38UCSC Ensembl
chr11:60472317..60472370hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6033170
Supporting Variants
Samples
Known GenesMS4A8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17592260
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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