A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516158



Internal ID20889519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:16482054..16485123hg38UCSC Ensembl
chr20:16462699..16465768hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg383070
hg193070
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066576
Samples
Known GenesKIF16B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516158
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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