A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761169



Internal ID20537029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92777667..92777667hg38UCSC Ensembl
chr15:93320897..93320897hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259841
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761169
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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