A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16282723



Internal ID20491941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60815387..60815566hg38UCSC Ensembl
chr11:60582860..60583039hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4747838
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16282723
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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