A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6040349



Internal ID21949692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116780154..116780272hg38UCSC Ensembl
chr11:116650870..116650988hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17614307
Samples
Known GenesZNF259
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6040349
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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