A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5644380



Internal ID21592685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:73014347..73014347hg38UCSC Ensembl
chr9:75629263..75629263hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38244
hg19244
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17162640
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5644380
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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