A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6061185



Internal ID21970418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151644234..151644234hg38UCSC Ensembl
chr3:151362022..151362022hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg386040
hg196040
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17554770
Samples
Known GenesMIR548H2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6061185
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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