A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5671761



Internal ID21620068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:47613316..47613316hg38UCSC Ensembl
chr22:48009065..48009065hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17135447
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5671761
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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