A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4444150



Internal ID22110330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113624319..113624319hg38UCSC Ensembl
chr13:114278634..114278634hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38626
hg19626
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15761928
Samples
Known GenesTFDP1
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4444150
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