A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5895693



Internal ID22670779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:109393274..109396238hg38UCSC Ensembl
chr3:109112121..109115085hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg382965
hg192965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17402555
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5895693
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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