A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5662717



Internal ID21611022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63927776..63927776hg38UCSC Ensembl
chr11:63695248..63695248hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17075624
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5662717
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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