A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497745



Internal ID20870953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:22070002..22070416hg38UCSC Ensembl
chr16:22081323..22081737hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38415
hg19415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028871
Samples
Known GenesC16orf52
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497745
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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