A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4441563



Internal ID22107744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14774688..14774688hg38UCSC Ensembl
chr19:14885500..14885500hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15765589
Samples
Known GenesEMR2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4441563
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