A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5899197



Internal ID22674324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43177722..43177883hg38UCSC Ensembl
chr5:43177824..43177985hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17423692
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5899197
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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