A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6059012



Internal ID21968245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:47312723..47312723hg38UCSC Ensembl
chr1:47778395..47778395hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17531889
Samples
Known GenesSTIL
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6059012
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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