A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6055975



Internal ID21965208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:183481866..183481866hg38UCSC Ensembl
chr1:183451001..183451001hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg382602
hg192602
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17521347
Samples
Known GenesSMG7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6055975
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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