A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418909



Internal ID21076462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135444624..135458316hg38UCSC Ensembl
chr7:135129372..135143064hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3813693
hg1913693
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18152346
Samples
Known GenesCNOT4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418909
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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