A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6092085



Internal ID22001318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111800317..111800317hg38UCSC Ensembl
chr11:111671041..111671041hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg382591
hg192591
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17613418
Samples
Known GenesALG9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6092085
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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