A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5644571



Internal ID21592876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:113935454..113935454hg38UCSC Ensembl
chr11:113806176..113806176hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17072185
SamplesHG00512
Known GenesHTR3B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5644571
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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