A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17586666



Internal ID21778709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9706035..9706248hg38UCSC Ensembl
chr11:9727582..9727795hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38214
hg19214
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6026675
Supporting Variants
Samples
Known GenesSWAP70
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17586666
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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