A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511351



Internal ID20884678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11154528..11161839hg38UCSC Ensembl
chr16:11248385..11255696hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg387312
hg197312
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028322
Samples
Known GenesCLEC16A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511351
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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