A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503417



Internal ID20876672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69121580..69122475hg38UCSC Ensembl
chr16:69155483..69156378hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38896
hg19896
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031764
Samples
Known GenesCHTF8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503417
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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