A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6098599



Internal ID22007832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47401003..47401003hg38UCSC Ensembl
chr11:47422554..47422554hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587104
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6098599
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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