A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15745716



Internal ID21392818
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 StatusS
Merged Variantsnsv4434480
Supporting Variants
SamplesSMI041
Known GenesTNFAIP8
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15745716
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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