A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267940



Internal ID20477158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1967753..1967811hg38UCSC Ensembl
chr19:1967752..1967810hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4748124
Supporting Variants
Samples
Known GenesCSNK1G2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267940
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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