A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17621934



Internal ID21813981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:5144433..5144433hg38UCSC Ensembl
chr19:5144444..5144444hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6109698
Supporting Variants
Samples
Known GenesKDM4B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17621934
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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