A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434635



Internal ID21396637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:3321887..3324886hg38UCSC Ensembl
chr5:3322001..3325000hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15752910, nssv15752373
SamplesNB11, NB07
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434635
Frequency
Sample Size15
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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