A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6033170



Internal ID21942513
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 StatusM
Merged Variants
Supporting Variantsnssv17592260
Samples
Known GenesMS4A8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6033170
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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