A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6022914



Internal ID21932257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35895372..35895464hg38UCSC Ensembl
chr11:35916922..35917014hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17580233
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6022914
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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