A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5891059



Internal ID22666092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:112112957..112113047hg38UCSC Ensembl
chr4:113034113..113034203hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425576
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5891059
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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