A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5636075



Internal ID21584380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:115095598..115095598hg38UCSC Ensembl
chr9:117857877..117857877hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17160248
SamplesHG02587
Known GenesTNC
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5636075
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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