A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027533



Internal ID21936876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33929270..33929370hg38UCSC Ensembl
chr11:33950817..33950917hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17589805
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027533
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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