A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4441598



Internal ID22107779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18116767..18116767hg38UCSC Ensembl
chr19:18227577..18227577hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38355
hg19355
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15767477
Samples
Known GenesMAST3
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4441598
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer