A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6057269



Internal ID21966502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109298698..109298698hg38UCSC Ensembl
chr1:109841320..109841320hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517573
Samples
Known GenesMYBPHL
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6057269
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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