A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4439955



Internal ID22106132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141599751..141599751hg38UCSC Ensembl
chr3:141318593..141318593hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38346
hg19346
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15759630
Samples
Known GenesRASA2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4439955
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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