A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503798



Internal ID20877054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66987992..66991227hg38UCSC Ensembl
chr16:67021895..67025130hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg383236
hg193236
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190276
Samples
Known GenesCES4A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503798
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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