A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6058273



Internal ID21967507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:222645833..222645833hg38UCSC Ensembl
chr1:222819175..222819175hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17518625
Samples
Known GenesMIA3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6058273
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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