A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17588800



Internal ID21780843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59706572..59706729hg38UCSC Ensembl
chr11:59474045..59474202hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6024228
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17588800
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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