A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027430



Internal ID21936773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96399533..96399608hg38UCSC Ensembl
chr11:96132697..96132772hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583551
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027430
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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