A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17073873



Internal ID21484805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2367226..2367297hg38UCSC Ensembl
chr11:2388456..2388527hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5603420
Supporting Variants
SamplesNA12329
Known GenesCD81-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17073873
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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