A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434622



Internal ID21396624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2207887..2211886hg38UCSC Ensembl
chr5:2208001..2212000hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg384000
hg194000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv626n172
Supporting Variantsnssv15748623
SamplesMDQ010
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434622
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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