A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5630603



Internal ID21578908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132269892..132269892hg38UCSC Ensembl
chr9:135145279..135145279hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17160384
SamplesNA19650
Known GenesSETX
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5630603
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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