A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17389876



Internal ID22447746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:16318104..16318162hg38UCSC Ensembl
chr20:16298749..16298807hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5941446
Supporting Variants
Samples
Known GenesKIF16B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17389876
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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