A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17072379



Internal ID21506017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10866131..10866181hg38UCSC Ensembl
chr11:10887678..10887728hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5586940
Supporting Variants
SamplesNA19983
Known GenesZBED5-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17072379
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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