A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397963



Internal ID21055516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:180443802..180540304hg38UCSC Ensembl
chr5:179870802..179967304hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3896503
hg1996503
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215137
Samples
Known GenesCNOT6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397963
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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