A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16277911



Internal ID20487129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:57658910..57659359hg38UCSC Ensembl
chr11:57426382..57426831hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38450
hg19450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4735731
Supporting Variants
Samples
Known GenesCLP1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16277911
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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