A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5653793



Internal ID21602098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61377729..61377729hg38UCSC Ensembl
chr11:61145201..61145201hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17074868
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5653793
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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