A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16263783



Internal ID20473001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59298746..59298804hg38UCSC Ensembl
chr11:59066219..59066277hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4742106
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16263783
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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