A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511066



Internal ID20884391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4738749..4773775hg38UCSC Ensembl
chr16:4788750..4823776hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3835027
hg1935027
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029721
Samples
Known GenesC16orf71, ZNF500
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511066
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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