A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4442728



Internal ID22108911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:11009487..11009487hg38UCSC Ensembl
chr20:10990135..10990135hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38406
hg19406
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15766067
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4442728
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