A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5651481



Internal ID21599786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:70411408..70411408hg38UCSC Ensembl
chr11:70257514..70257514hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17075519
SamplesHG02011
Known GenesCTTN
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5651481
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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