A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4448854



Internal ID22115032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:29660535..29660535hg38UCSC Ensembl
chr8:29518051..29518051hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15763882
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4448854
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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