A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17074378



Internal ID21413068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:36144698..36144784hg38UCSC Ensembl
chr11:36166248..36166334hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5603983
Supporting Variants
SamplesHG00513
Known GenesLDLRAD3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17074378
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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