A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6030288



Internal ID21939631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69424000..69619823hg38UCSC Ensembl
chr11:69238768..69434591hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg38195824
hg19195824
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585047
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6030288
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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