A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5664000



Internal ID21612305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122182844..122182844hg38UCSC Ensembl
chr11:122053552..122053552hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17072918
SamplesNA12878
Known GenesMIR100HG
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5664000
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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