A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6055063



Internal ID21964296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:56556958..56556958hg38UCSC Ensembl
chr1:57022631..57022631hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17527331
Samples
Known GenesPPAP2B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6055063
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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