A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4440379



Internal ID22106557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:183684813..183684813hg38UCSC Ensembl
chr3:183402601..183402601hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg381535
hg191535
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15758394
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4440379
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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