A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5671724



Internal ID21620031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:45238875..45238875hg38UCSC Ensembl
chr22:45634756..45634756hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17122787
SamplesHG03486
Known GenesKIAA0930
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5671724
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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