A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5595552



Internal ID21544158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132986227..132986279hg38UCSC Ensembl
chr9:135861614..135861666hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17160153
SamplesHG03065
Known GenesGFI1B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5595552
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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