A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6028608



Internal ID21937951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:130049210..130054361hg38UCSC Ensembl
chr11:129919105..129924256hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg385152
hg195152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602031
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6028608
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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