A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509412



Internal ID20882721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:56655681..56662421hg38UCSC Ensembl
chr16:56689593..56696333hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg386741
hg196741
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18030234
Samples
Known GenesMT1F
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509412
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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