A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5653329



Internal ID21601634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:15113119..15113119hg38UCSC Ensembl
chr11:15134665..15134665hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17073223
SamplesNA19238
Known GenesINSC
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5653329
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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