A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17582003



Internal ID21774046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:12375940..12377403hg38UCSC Ensembl
chr11:12397487..12398950hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg381464
hg191464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6030093
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17582003
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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