A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515131



Internal ID20888489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3297483..3303851hg38UCSC Ensembl
chr16:3347483..3353851hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg386369
hg196369
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029836
Samples
Known GenesTIGD7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515131
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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