A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4439918



Internal ID22106095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:48766875..48766875hg38UCSC Ensembl
chr18:46293246..46293246hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15755856
Samples
Known GenesCTIF
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4439918
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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