A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5893901



Internal ID22668968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:19092344..19097443hg38UCSC Ensembl
chr3:19133836..19138935hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg385100
hg195100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17418026
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5893901
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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