A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510941



Internal ID20884264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69409401..69502000hg38UCSC Ensembl
chr16:69443304..69535903hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3892600
hg1992600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031791
Samples
Known GenesCYB5B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510941
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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