A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522681



Internal ID20896042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:16377119..16412208hg38UCSC Ensembl
chr20:16357764..16392853hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3835090
hg1935090
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066568
Samples
Known GenesKIF16B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522681
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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