A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514212



Internal ID20887564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66543133..66546738hg38UCSC Ensembl
chr16:66577036..66580641hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg383606
hg193606
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031285
Samples
Known GenesTK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514212
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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