A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416403



Internal ID21073956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135463379..135468494hg38UCSC Ensembl
chr7:135148127..135153242hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg385116
hg195116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18152352
Samples
Known GenesCNOT4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416403
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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