A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5901508



Internal ID22676659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160326312..160326474hg38UCSC Ensembl
chr3:160044100..160044262hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg38163
hg19163
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17410034
Samples
Known GenesIFT80
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5901508
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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