A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6055542



Internal ID21964775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:193665628..193665628hg38UCSC Ensembl
chr1:193634758..193634758hg19UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg381716
hg191716
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17519739
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6055542
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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