A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5629391



Internal ID21577696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96160187..96160187hg38UCSC Ensembl
chr9:98922469..98922469hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17163165
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5629391
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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