A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17075608



Internal ID21471275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63378230..63378230hg38UCSC Ensembl
chr11:63145702..63145702hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5649260
Supporting Variants
SamplesHG03125
Known GenesMIR3680-1, MIR3680-2, SLC22A9
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17075608
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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