A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5895640



Internal ID22670725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72588938..72590361hg38UCSC Ensembl
chr3:72638089..72639512hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg381424
hg191424
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17429628
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5895640
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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