A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902489



Internal ID22677648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:109847485..109847607hg38UCSC Ensembl
chr4:110768641..110768763hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425606
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902489
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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