A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17519033



Internal ID21843392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:43593626..43593626hg38UCSC Ensembl
chr1:44059297..44059297hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38474
hg19474
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6040969
Supporting Variants
Samples
Known GenesPTPRF
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17519033
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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