A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17076058



Internal ID21444469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74139909..74139909hg38UCSC Ensembl
chr11:73850954..73850954hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5655352
Supporting Variants
SamplesHG00732
Known GenesC2CD3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17076058
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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