A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5595061



Internal ID21543663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133105836..133105895hg38UCSC Ensembl
chr9:135981223..135981282hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17159796
SamplesHG00731
Known GenesRALGDS
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5595061
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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