A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4446842



Internal ID22113019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101925705..101925705hg38UCSC Ensembl
chr11:101796436..101796436hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38817
hg19817
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15768240
Samples
Known GenesKIAA1377
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4446842
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