A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980707



Internal ID21890050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10372564..10372637hg38UCSC Ensembl
chr1:10432622..10432695hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17520404
Samples
Known GenesKIF1B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5980707
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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