A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051925



Internal ID21961158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84486120..84486120hg38UCSC Ensembl
chr1:84951803..84951803hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17524169
Samples
Known GenesRPF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051925
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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