A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5648076



Internal ID21596381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77706997..77706997hg38UCSC Ensembl
chr11:77418042..77418042hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38282
hg19282
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17075716
SamplesHG02587
Known GenesRSF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5648076
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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