A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051491



Internal ID21960724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:56554437..56554437hg38UCSC Ensembl
chr1:57020110..57020110hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg38160
hg19160
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17518018
Samples
Known GenesPPAP2B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051491
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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