A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101108



Internal ID22010341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:313118..313118hg38UCSC Ensembl
chr19:313118..313118hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17617746
Samples
Known GenesMIER2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101108
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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