A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4439084



Internal ID22105261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:13672960..13672960hg38UCSC Ensembl
chr18:13672959..13672959hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38513
hg19513
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15759708
Samples
Known GenesFAM210A
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4439084
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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