A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508464



Internal ID20881765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67008596..67010742hg38UCSC Ensembl
chr16:67042499..67044645hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg382147
hg192147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031324
Samples
Known GenesCES4A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508464
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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