A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5596522



Internal ID21545130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35803099..35803401hg38UCSC Ensembl
chr9:35803096..35803398hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17161720
SamplesHG00513
Known GenesNPR2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5596522
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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