A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4446187



Internal ID22112366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62784008..62784008hg38UCSC Ensembl
chr11:62551480..62551480hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15763402
Samples
Known GenesTAF6L
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4446187
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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