A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024793



Internal ID21934136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60762431..60762841hg38UCSC Ensembl
chr11:60529904..60530314hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38411
hg19411
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17592616
Samples
Known GenesMS4A15
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024793
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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