A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4437293



Internal ID22103472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:167350761..167350761hg38UCSC Ensembl
chr5:166777766..166777766hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15757336
Samples
Known GenesTENM2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4437293
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