A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4446559



Internal ID22112737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:42349653..42349653hg38UCSC Ensembl
chr21:43769762..43769762hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15763777
Samples
Known GenesTFF2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4446559
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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