A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503661



Internal ID20876917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67053201..67055100hg38UCSC Ensembl
chr16:67087104..67089003hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031326
Samples
Known GenesCBFB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503661
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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