A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905423



Internal ID22680610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4030576..4133717hg38UCSC Ensembl
chr3:4072260..4175401hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38103142
hg19103142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1439n209
Supporting Variantsnssv17419548
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905423
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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