A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027909



Internal ID21937252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65842774..65843049hg38UCSC Ensembl
chr11:65610245..65610520hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38276
hg19276
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593247
Samples
Known GenesSNX32
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027909
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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