A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6088476



Internal ID21997709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:131123..131123hg38UCSC Ensembl
chr11:186364..186364hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17628669
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6088476
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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