A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877030



Internal ID22651993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:3884104..3887849hg38UCSC Ensembl
chr1:3800668..3804413hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg383746
hg193746
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17372088
Samples
Known GenesDFFB
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877030
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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