A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515276



Internal ID20888635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:52499901..52501300hg38UCSC Ensembl
chr16:52533813..52535212hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18030399
Samples
Known GenesTOX3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515276
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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