A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408827



Internal ID21066380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:90394148..90394570hg38UCSC Ensembl
chr5:89689965..89690387hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38423
hg19423
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18134919
Samples
Known GenesCETN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408827
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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