A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5949077



Internal ID22666301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:22368385..22368385hg38UCSC Ensembl
chr4:22370008..22370008hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38255
hg19255
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428235
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5949077
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer