A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434029



Internal ID21396031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:196898130..196900129hg38UCSC Ensembl
chr3:196625001..196627000hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15747500
SamplesBTQ016
Known GenesSENP5
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434029
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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