A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15181898



Internal ID21320694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:125426489..125426614hg38UCSC Ensembl
chr11:125296385..125296510hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3926635
Supporting Variants
SamplesHG002
Known GenesPKNOX2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15181898
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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