A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051335



Internal ID21960569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:210304854..210304854hg38UCSC Ensembl
chr1:210478199..210478199hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg38290
hg19290
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17519557
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051335
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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