A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5632661



Internal ID21580966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:13605521..13605521hg38UCSC Ensembl
chr9:13605520..13605520hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17160876
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5632661
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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