A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4446098



Internal ID22112277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:18411077..18411077hg38UCSC Ensembl
chr2:18592343..18592343hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg38352
hg19352
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15768400
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4446098
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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