A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406783



Internal ID21064336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:152162336..152171772hg38UCSC Ensembl
chr5:151541897..151551333hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg389437
hg199437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18126968
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406783
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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