A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5894773



Internal ID22669848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:45212092..45303043hg38UCSC Ensembl
chr4:45214109..45305060hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3890952
hg1990952
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425493
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5894773
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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