A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6092311



Internal ID22001544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77583925..77583925hg38UCSC Ensembl
chr11:77294970..77294970hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584442
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6092311
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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