A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101886



Internal ID22011119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:13769976..13769976hg38UCSC Ensembl
chr19:13880790..13880790hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38291
hg19291
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635205
Samples
Known GenesMRI1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101886
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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