A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6055659



Internal ID21964892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26369673..26369673hg38UCSC Ensembl
chr1:26696164..26696164hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17532824
Samples
Known GenesZNF683
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6055659
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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