A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399490



Internal ID21057043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:160317721..160329619hg38UCSC Ensembl
chr5:159744728..159756626hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3811899
hg1911899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215930
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399490
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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