A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896239



Internal ID22671328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:131418863..131418912hg38UCSC Ensembl
chr5:130754556..130754605hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17410482
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5896239
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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