A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4445512



Internal ID22111691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:81010864..81010864hg38UCSC Ensembl
chr14:81477208..81477208hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg386017
hg196017
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15760877
Samples
Known GenesTSHR
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4445512
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