A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17592060



Internal ID21784103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32117855..32117975hg38UCSC Ensembl
chr11:32139401..32139521hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6025146
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17592060
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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