A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6031479



Internal ID21940822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:129862837..129863442hg38UCSC Ensembl
chr11:129732732..129733337hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38606
hg19606
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17616627
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6031479
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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