A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5904928



Internal ID22680108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:143031405..143031470hg38UCSC Ensembl
chr3:142750247..142750312hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17403219
Samples
Known GenesU2SURP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5904928
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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