A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060105



Internal ID21969338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:117386725..117386725hg38UCSC Ensembl
chr1:117929347..117929347hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17522795
Samples
Known GenesMAN1A2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060105
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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