A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4448886



Internal ID22115064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:31278832..31278832hg38UCSC Ensembl
chr8:31136348..31136348hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15758962
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4448886
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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