A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665150



Internal ID21613455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:26661919..26661919hg38UCSC Ensembl
chr22:27057883..27057883hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17134707
SamplesHG00512
Known GenesMIAT
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665150
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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