A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6052207



Internal ID21961440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:55003057..55003057hg38UCSC Ensembl
chr1:55468730..55468730hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38575
hg19575
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17532879
Samples
Known GenesBSND
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6052207
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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