A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16280021



Internal ID20489239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64270932..64271004hg38UCSC Ensembl
chr11:64038404..64038476hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4741511
Supporting Variants
Samples
Known GenesBAD
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16280021
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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