A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16293061



Internal ID20502279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76250830..76257310hg38UCSC Ensembl
chr11:75961874..75968354hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg386481
hg196481
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4749612
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16293061
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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