A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4440807



Internal ID22106985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:34506225..34506225hg38UCSC Ensembl
chr13:35080362..35080362hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15764088
Samples
Known GenesLINC00457
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4440807
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