A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5633445



Internal ID21581750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132997579..132997579hg38UCSC Ensembl
chr9:135872966..135872966hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17159787
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5633445
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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