A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17606309



Internal ID21798356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:130092181..130092299hg38UCSC Ensembl
chr11:129962076..129962194hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6020948
Supporting Variants
Samples
Known GenesAPLP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17606309
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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