A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6043927



Internal ID21953218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8862583..8862583hg38UCSC Ensembl
chr1:8922642..8922642hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17533664
Samples
Known GenesENO1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6043927
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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