A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903742



Internal ID22678911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:55064189..55065172hg38UCSC Ensembl
chr4:55930356..55931339hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38984
hg19984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17423199
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903742
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