A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17587355



Internal ID21779398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:28429790..28430100hg38UCSC Ensembl
chr11:28451337..28451647hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6021925
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17587355
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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