A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17987325



Internal ID20554367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126139241..126139677hg38UCSC Ensembl
chr11:126009136..126009572hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38437
hg19437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6463210
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17987325
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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