A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4446279



Internal ID22112458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68264321..68264321hg38UCSC Ensembl
chr11:68031789..68031789hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38767
hg19767
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15760361
Samples
Known GenesC11orf24
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4446279
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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