A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5638580



Internal ID21586885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:120870766..120870766hg38UCSC Ensembl
chr9:123633044..123633044hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38496
hg19496
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17159708
SamplesHG02587
Known GenesPHF19
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5638580
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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