A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900850



Internal ID22675997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:176675997..176693277hg38UCSC Ensembl
chr5:176102998..176120278hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3817281
hg1917281
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415840
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900850
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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