A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051244



Internal ID21960477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:205737821..205737821hg38UCSC Ensembl
chr1:205706949..205706949hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg382603
hg192603
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17520511
Samples
Known GenesNUCKS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051244
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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