A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4445141



Internal ID22111321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:13016422..13016422hg38UCSC Ensembl
chr11:13037969..13037969hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38173
hg19173
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15755975
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4445141
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