A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4446924



Internal ID22113101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69285997..69285997hg38UCSC Ensembl
chr15:69578336..69578336hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15766402
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4446924
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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