A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5895683



Internal ID22670769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:148879409..148881323hg38UCSC Ensembl
chr4:149800561..149802475hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg381915
hg191915
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424070
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5895683
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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