A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5661031



Internal ID21609336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:71387784..71387784hg38UCSC Ensembl
chr11:71098830..71098830hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17075949
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5661031
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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