A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381145



Internal ID21038698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:9725675..9770652hg38UCSC Ensembl
chr5:9725787..9770764hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3844978
hg1944978
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215442
Samples
Known GenesLOC285692
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381145
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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