A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497773



Internal ID20870981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67097111..67097522hg38UCSC Ensembl
chr16:67131014..67131425hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38412
hg19412
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031331
Samples
Known GenesCBFB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497773
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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