A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4447319



Internal ID22113496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80911950..80911950hg38UCSC Ensembl
chr15:81204291..81204291hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15759917
Samples
Known GenesKIAA1199
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4447319
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