A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17577855



Internal ID21769898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69759207..69759264hg38UCSC Ensembl
chr11:69573975..69574032hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6022298
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17577855
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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