A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6078810



Internal ID21988043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:169782022..169782022hg38UCSC Ensembl
chr3:169499810..169499810hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg381276
hg191276
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17543407
Samples
Known GenesMYNN
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6078810
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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