A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5596251



Internal ID21544858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:39426483..39426863hg38UCSC Ensembl
chr9:39426480..39426860hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38381
hg19381
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17161680
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5596251
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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