A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4448652



Internal ID22114829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98437709..98437709hg38UCSC Ensembl
chr15:98980938..98980938hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15762883
Samples
Known GenesFAM169B
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4448652
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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