A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5630369



Internal ID21578674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91347963..91347963hg38UCSC Ensembl
chr9:94110245..94110245hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17163392
SamplesHG00513
Known GenesAUH
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5630369
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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