A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5653770



Internal ID21602075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59565870..59565870hg38UCSC Ensembl
chr11:59333343..59333343hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17075545
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5653770
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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