A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5888354



Internal ID22663359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:174556173..174586011hg38UCSC Ensembl
chr4:175477324..175507162hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3829839
hg1929839
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17426858
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5888354
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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