A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5642564



Internal ID21590869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97144644..97144644hg38UCSC Ensembl
chr9:99906926..99906926hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17163398
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5642564
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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