A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5643272



Internal ID21591577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130901254..130901254hg38UCSC Ensembl
chr9:133776641..133776641hg19UCSC Ensembl
Cytoband9q34.12
Allele length
AssemblyAllele length
hg382993
hg192993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17160120
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5643272
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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