A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6099770



Internal ID22009003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126183174..126183174hg38UCSC Ensembl
chr11:126053069..126053069hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38276
hg19276
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17616454
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6099770
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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