A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434480



Internal ID21396482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:119265306..119348305hg38UCSC Ensembl
chr5:118601001..118684000hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3883000
hg1983000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15745716
SamplesSMI041
Known GenesTNFAIP8
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434480
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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