A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6090527



Internal ID21999760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:70017470..70017470hg38UCSC Ensembl
chr11:69863576..69863576hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583902
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6090527
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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