A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17620841



Internal ID21812888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:90217..90360hg38UCSC Ensembl
chr11:152420..152563hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6020475
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17620841
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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