A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17073140



Internal ID21490047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134092275..134092334hg38UCSC Ensembl
chr11:133962170..133962229hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5587793
Supporting Variants
SamplesNA19238
Known GenesJAM3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17073140
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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