A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17073027



Internal ID21437452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118875642..118875723hg38UCSC Ensembl
chr11:118746351..118746432hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5594752
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17073027
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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