A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17614573



Internal ID21806620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:117264951..117265024hg38UCSC Ensembl
chr11:117135667..117135740hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6031135
Supporting Variants
Samples
Known GenesRNF214
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17614573
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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